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11q23.3-q25CNV Type: Deletion


Largest CNV size: 14700000 bp

Statistics Box:
Number of Reports: 5



Summary Information

Summary statement in development

Additional Locus Information

Genome browsers

USCS Symbol             NCBI Symbol

Decipher

            Decipher Symbol

References

Major Reports

Title
Author, Year
Report Class
CNV Type
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabili...
Deletion-Duplication

Minor Reports

Title
Author, Year
Report Class
CNV Type
The clinical utility of molecular karyotyping using high-resolution array-comparative genomic hybridization.
Deletion
Genomic diagnosis for children with intellectual disability and/or developmental delay.
Duplication
Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights.
Duplication

Cases

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 akshoomoff_14_ASD_discovery_cases
 17 patients with Jacobsen syndrome (11q terminal deletion disorder), prospectively recruited from the 11q Research and Resource Group; and 3 additional patients with atypical distal 11q deletions
 20
 Diagnosis of ASD assessed using ADOS (n=18) or ADI-R (n=2). Cognitive abilities in cases assessed using the Bayley Scales of Infant and Toddler Development, Third Edition; the Differential Ability Scales; the Wechsler Intelligence Scale for Children, Fourth Edition; or the Wechsler Adult Intelligence Scale, Fourth Edition.
 Range, 3.8-21.9 yrs.
 20.0% Male
 14600000
 4
 0
 4
 bowling_17_DD/ID_discovery_cases
 Individuals affected by developmental delay and/or intellectual disability and enrolled at North Alabama Children's Specialists (Huntsville, Alabama, USA)
 371
 Developmental delay (DD) and/or intellectual disability (ID); seizures in 45.3% of cases, ASD in 25.6% of cases
 Average age of 10.56 yrs. (range: 2-54 yrs.)
 57.7% Male
 16207934
 0
 1
 1
 kaminsky_11_DD/ID/ASD_discovery_cases
 Cases from the International Standards for Cytogenomic Arrays (ISCA) consortium
 15749
 Unexplained developmental delay, intellectual disability, dysmorphic features, multiple congenital anomalies, autism spectrum disorders, or clinical features suggestive of a chromosomal syndrome
 NA
 NA
 18146296
 3
 3
 6
 kushima_18_SCZ_discovery_cases
 Individuals predominantly recruited from the middle of Honshu Island (Japan)
 2458
 Cases were diagnosed with schizophrenia (SCZ) according to DSM-5 criteria.
 Median age, 44 years
 55.0% Male
 16087249
 0
 1
 1
 tzetis_12_DD/ID_discovery_cases
 Patients referred for aCGH analysis from 2008-present
 334
 Cases presented with at least one of the following clinical indications: developmental delay (DD), intellectual disability (ID), dysmorphic features, unique or multiple congenital anomalies (MCA), growth disorder, behavior disorder, and/or autism (ASD)
 Range, 1 month-38 years (median age of 4 years)
 
 14700000
 1
 0
 1

Controls

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 kaminsky_11_DD/ID/ASD_discovery_controls
 Controls from the International Standards for Cytogenomic Arrays (ISCA) consortium
 10118
 Controls
 NA
 NA
 NA
 NA
 NA
 NA
 kushima_18_ASD/SCZ_discovery_controls
 Individuals selected from the general population and predominantly recruited from the middle of Honshu Island (Japan)
 2095
 Controls had no history of mental disorders based upon responses to questionnaires or self-reporting.
 Median age, 37 years
 52.0% Male
 0
 0
 0
 0

Cases

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
 akshoomoff_14_ASD_discovery_cases
  N/A
 aCGH
  Signature Genomics custom-designed OS V2.0
 
 
 None
 bowling_17_DD/ID_discovery_cases
  N/A
 CMA, WGS
  Microarray platform N/A, WGS platform Illumina HiSeq Xs
 
 
 None
 kaminsky_11_DD/ID/ASD_discovery_cases
  NA
 aCGH
  Agilent 44K, Agilent 105K
 
 Feature Extraction, DNA Analytics
 FISH, qPCR, MLPA, aCGH, standard G-banded chromosome analysis
 kushima_18_SCZ_discovery_cases
  Japanese
 aCGH
  NimbleGen 720K, Agilent 400K
 FASST2
 Nexus Copy Number v.9.0
 N/A
 tzetis_12_DD/ID_discovery_cases
  Greece
 aCGH
  Agilent 244K, Agilent 4x180K
 ADM-1
 Agilent Feature Extraction V9.1, Agilent CGH Analytics V4.0, Illumina GenomeStudio V2011.1
 None

Controls

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
  kaminsky_11_DD/ID/ASD_discovery_controls
  NA
  aCGH
  Agilent 44K, Agilent 105K
 
  Feature Extraction, DNA Analytics
 
  kushima_18_ASD/SCZ_discovery_controls
  Japanese
  aCGH
  NimbleGen 720K, Agilent 400K
  FASST2
  Nexus Copy Number v.9.0
  N/A

Cases

Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
  akshoomoff_14_ASD_discovery_cases-patient14
 7.8 yrs.
 F
 Jacobsen syndrome
 Research diagnosis: non-spectrum. ADOS classification: non-spectrum. SCQ score above cutoff: yes.
 IQ estimate: 30 (test given: Differential Ability Scales, Preschool Version). VABS-II composite score: 64.
 120890746
 135006516 (approximate endpoint)
  14000000
 Unknown
 Deletion
 No
  akshoomoff_14_ASD_discovery_cases-patient15
 10.0 yrs.
 F
 Jacobsen syndrome
 Research diagnosis: non-spectrum. ADOS classification: non-spectrum. SCQ score above cutoff: yes.
 IQ estimate: 32 (test given: Differential Ability Scales). VABS-II composite score: 55.
 120771125
 135006516 (approximate endpoint)
  14100000
 Unknown
 Deletion
 No
  akshoomoff_14_ASD_discovery_cases-patient16
 11.7 yrs.
 F
 ASD and Jacobsen syndrome
 Research diagnosis: ASD. ADOS classification: autism. SCQ score above cutoff: yes.
 IQ estimate: 31 (test given: Differential Ability Scales, Preschool Version). VABS-II composite score: 51.
 120584320
 135006516 (approximate endpoint)
  14300000
 Unknown
 Deletion
 No
  akshoomoff_14_ASD_discovery_cases-patient17
 6.4 yrs.
 F
 ASD and Jacobsen syndrome
 Research diagnosis: ASD. ADOS classification: autism. SCQ score above cutoff: yes.
 IQ estimate: 44 (test given: Differential Ability Scales, Preschool Version). VABS-II composite score: 57.
 120288803
 135006516 (approximate endpoint)
  14600000
 Unknown
 Deletion
 No
  bowling_17_DD/ID_discovery_cases-case00123-C
 N/A
 N/A
 Intellectual disability and epilepsy
 Intellectual disability (moderate); Seizures: Speech delay; MRI Brain: normal; Decreased muscle tone (mild); Bilateral mid foot collapse (L>R); Calcaneal eversion (L>R); Lack of coordination and balance weakness; Significant gross motor delays
 Moderate intellectual disability
 118789765
 134998513
  16208749
 GRCh38
 Duplication
 No
  kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00000862
 NA
 NA
 Developmental delay/intellectual disability/ASD
 Clinical profile NA
 Cognitive profile NA
 116851395
 134998513
  18147119
 GRCh38
 Duplication
 Yes
  kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00000903
 NA
 NA
 Developmental delay/intellectual disability/ASD
 Clinical profile NA
 Cognitive profile NA
 119433909
 134998513
  15564605
 GRCh38
 Deletion
 Yes
  kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00001146
 NA
 NA
 Developmental delay/intellectual disability/ASD
 Clinical profile NA
 Cognitive profile NA
 118789765
 134998513
  16208749
 GRCh38
 Duplication
 Yes
  kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004178
 NA
 NA
 Developmental delay/intellectual disability/ASD
 Clinical profile NA
 Cognitive profile NA
 120236432
 135040246
  14803815
 GRCh38
 Duplication
 Yes
  kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004549
 NA
 NA
 Developmental delay/intellectual disability/ASD
 Clinical profile NA
 Cognitive profile NA
 119215032
 134998654
  15783623
 GRCh38
 Deletion
 Yes
  kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004702
 NA
 NA
 Developmental delay/intellectual disability/ASD
 Clinical profile NA
 Cognitive profile NA
 120507265
 134576266
  14069002
 GRCh38
 Deletion
 Yes
  kushima_18_SCZ_discovery_cases-caseSCZ0616
 60 yrs.
 M
 Schizophrenia
 No additional clinical information reported for this individual. Family history: unknown.
 
 118989374
 135076622
  16087249
 GRCh38
 Duplication
 N/A
  tzetis_12_DD/ID_discovery_cases-case31
 
 F
 DD/ID
 Flattened nasal ridge, upturned nasal tip, macrocephaly, small ears, hypoplastic small lips, thrombocytopenia, pulmonary artery stenosis, ventricular septal defect, captodactyly, short overlapping toes
 
 120359696
 135057220
  14697525
 GRCh38
 Deletion
 No

Controls

No Control Data Available

Cases

Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
 akshoomoff_14_ASD_discovery_cases-patient14
 
 
 Unknown
 Unknown
 Unknown
 Estimated gene content: TBCEL,TECTA,SC5D,SORL1,BLID,UBASH3B,CRTAM,C11orf63,BSX,HSPA8,CLMP,GRAMD1B,SCN3B,ZNF202,OR6X1,OR6M1,TMEM225,OR8D4,OR4D5,OR6T1,OR10S1,OR10G4,OR10G9,OR10G8,OR10G7,VWA5A,OR8G2,OR8G1,OR8G5,OR8D1,OR8D2,OR8B2,OR8B3,OR8B4,OR8B8,OR8B12,OR8A1,PANX3,TBRG1,SIAE,SPA17,NRGN,VSIG2,ESAM,MSANTD2,ROBO3,ROBO4,HEPACAM,HEPN1,CCDC15,SLC37A2,TMEM218,PKNOX2,FEZ1,EI24,STT3A,CHEK1,ACRV1,PATE1,PATE2,PATE3,PATE4,HYLS1,PUS3,DDX25,CDON,RPUSD4,FAM118B,SRPR,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3,ETS1,FLI1,KCNJ1,KCNJ5,C11orf45,TP53AIP1,ARHGAP32,BARX2,TMEM45B,NFRKB,PRDM10,APLP2,ST14,ZBTB44,ADAMTS8,ADAMTS15,C11orf44,SNX19,NTM,OPCML,SPATA19,IGSF9B,JAM3,NCAPD3,VPS26B,THYN1,ACAD8,GLB1L3,GLB1L2,B3GAT1
 
 akshoomoff_14_ASD_discovery_cases-patient15
 
 
 Unknown
 Unknown
 Unknown
 Estimated gene content: GRIK4,TBCEL,TECTA,SC5D,SORL1,BLID,UBASH3B,CRTAM,C11orf63,BSX,HSPA8,CLMP,GRAMD1B,SCN3B,ZNF202,OR6X1,OR6M1,TMEM225,OR8D4,OR4D5,OR6T1,OR10S1,OR10G4,OR10G9,OR10G8,OR10G7,VWA5A,OR8G2,OR8G1,OR8G5,OR8D1,OR8D2,OR8B2,OR8B3,OR8B4,OR8B8,OR8B12,OR8A1,PANX3,TBRG1,SIAE,SPA17,NRGN,VSIG2,ESAM,MSANTD2,ROBO3,ROBO4,HEPACAM,HEPN1,CCDC15,SLC37A2,TMEM218,PKNOX2,FEZ1,EI24,STT3A,CHEK1,ACRV1,PATE1,PATE2,PATE3,PATE4,HYLS1,PUS3,DDX25,CDON,RPUSD4,FAM118B,SRPR,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3,ETS1,FLI1,KCNJ1,KCNJ5,C11orf45,TP53AIP1,ARHGAP32,BARX2,TMEM45B,NFRKB,PRDM10,APLP2,ST14,ZBTB44,ADAMTS8,ADAMTS15,C11orf44,SNX19,NTM,OPCML,SPATA19,IGSF9B,JAM3,NCAPD3,VPS26B,THYN1,ACAD8,GLB1L3,GLB1L2,B3GAT1
 
 akshoomoff_14_ASD_discovery_cases-patient16
 
 
 Unknown
 Unknown
 Unknown
 Estimated gene content: GRIK4,TBCEL,TECTA,SC5D,SORL1,BLID,UBASH3B,CRTAM,C11orf63,BSX,HSPA8,CLMP,GRAMD1B,SCN3B,ZNF202,OR6X1,OR6M1,TMEM225,OR8D4,OR4D5,OR6T1,OR10S1,OR10G4,OR10G9,OR10G8,OR10G7,VWA5A,OR8G2,OR8G1,OR8G5,OR8D1,OR8D2,OR8B2,OR8B3,OR8B4,OR8B8,OR8B12,OR8A1,PANX3,TBRG1,SIAE,SPA17,NRGN,VSIG2,ESAM,MSANTD2,ROBO3,ROBO4,HEPACAM,HEPN1,CCDC15,SLC37A2,TMEM218,PKNOX2,FEZ1,EI24,STT3A,CHEK1,ACRV1,PATE1,PATE2,PATE3,PATE4,HYLS1,PUS3,DDX25,CDON,RPUSD4,FAM118B,SRPR,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3,ETS1,FLI1,KCNJ1,KCNJ5,C11orf45,TP53AIP1,ARHGAP32,BARX2,TMEM45B,NFRKB,PRDM10,APLP2,ST14,ZBTB44,ADAMTS8,ADAMTS15,C11orf44,SNX19,NTM,OPCML,SPATA19,IGSF9B,JAM3,NCAPD3,VPS26B,THYN1,ACAD8,GLB1L3,GLB1L2,B3GAT1
 
 akshoomoff_14_ASD_discovery_cases-patient17
 
 
 Unknown
 Unknown
 Unknown
 Estimated gene content: ARHGEF12,GRIK4,TBCEL,TECTA,SC5D,SORL1,BLID,UBASH3B,CRTAM,C11orf63,BSX,HSPA8,CLMP,GRAMD1B,SCN3B,ZNF202,OR6X1,OR6M1,TMEM225,OR8D4,OR4D5,OR6T1,OR10S1,OR10G4,OR10G9,OR10G8,OR10G7,VWA5A,OR8G2,OR8G1,OR8G5,OR8D1,OR8D2,OR8B2,OR8B3,OR8B4,OR8B8,OR8B12,OR8A1,PANX3,TBRG1,SIAE,SPA17,NRGN,VSIG2,ESAM,MSANTD2,ROBO3,ROBO4,HEPACAM,HEPN1,CCDC15,SLC37A2,TMEM218,PKNOX2,FEZ1,EI24,STT3A,CHEK1,ACRV1,PATE1,PATE2,PATE3,PATE4,HYLS1,PUS3,DDX25,CDON,RPUSD4,FAM118B,SRPR,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3,ETS1,FLI1,KCNJ1,KCNJ5,C11orf45,TP53AIP1,ARHGAP32,BARX2,TMEM45B,NFRKB,PRDM10,APLP2,ST14,ZBTB44,ADAMTS8,ADAMTS15,C11orf44,SNX19,NTM,OPCML,SPATA19,IGSF9B,JAM3,NCAPD3,VPS26B,THYN1,ACAD8,GLB1L3,GLB1L2,B3GAT1
 
 bowling_17_DD/ID_discovery_cases-case00123-C
 
 
 De novo
 
 Likely segregated
 SETP16,CXCR5,MIR4492,RPL23AP64,RPS25,TRAPPC4,HMBS,DPAGT1,PDZD3,RNU6-262P,MCAM,MIR6756,RNF26,C1QTNF5,DUXAP5,RNU6-1123P,TMEM136,ELOCP22,HMGB1P42,RPS4XP12,BMPR1AP2,RNU6-256P,MIR125B1,BLID,MIRLET7A2,MIR100,RNU4ATAC10P,RNU4ATAC5P,RNU6-592P,GLULP3,RNU4-23P,ATP5PBP5,RPL34P23,RPS26P43,RPL31P47,SNORD14E,SNORD14D,SNORD14C,PHBP17,MIR4493,SF3A3P2,OR6X1,RNU1-21P,OR6M1,OR6M2P,OR6M3P,TMEM225,OR8D4,OR4D5,OR6T1,OR10G6,OR10G5P,OR10G4,OR10G9,OR10G7,OR10D5P,OR10D4P,OR10D1P,OR10D3,OR8F1P,OR8G3P,OR8G2P,OR8G7P,OR8G1,OR8G5,SLC5A4P1,OR8D2,OR8B7P,OR8B6P,OR8B5P,OR8B1P,OR8C1P,OR8B2,OR8B3,OR8X1P,OR8B4,OR8B8,OR8A2P,OR8B9P,OR8B10P,OR8A3P,OR8B12,OR8Q1P,RNA5SP352,NRGN,ESAM,HEPN1,PKNOX2-AS1,RNU6-321P,RNU6-1156P,RNU2-35P,ACRV1,PATE2,PATE3,PATE4,VSIG10L2,NAP1L1P1,RNU4-86P,RN7SL351P,SRPRA,RPL35AP26,MIR3167,KIRREL3-AS3,RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,BCL9L,UPK2,RN7SL688P,FOXR1,SLC37A4,HYOU1,VPS11,H2AFX,C2CD2L,HINFP,ABCG4,NLRX1,CCDC153,MFRP,USP2,THY1,KRT8P7,TRIM29,OAF,POU2F3,TBCEL,SC5D,CRTAM,BSX,HSPA8,SCN3B,OR10S1,OR10G8,OR10N1P,OR8D1,OR8A1,PANX3,TBRG1,SPA17,VSIG2,ROBO3,ROBO4,HEPACAM,CCDC15,SLC37A2,TMEM218,KRT18P59,EI24,STT3A,CHEK1,PATE1,HYLS1,PUS3,DDX25,RPUSD4,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3-AS1,KIRREL3-AS2,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,DDX6,CCDC84,CBL,USP2-AS1,NECTIN1,ARHGEF12,TECTA,SORL1,MIR100HG,JHY,CLMP,GRAMD1B,VWA5A,SIAE,PKNOX2,FEZ1,CDON,FAM118B,GSEC,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,GRIK4,UBASH3B,ZNF202,MSANTD2,KIRREL3,ARHGAP32,NTM,OPCML,NCAPD3
 
 kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00000862
 FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
 
 Unknown
 Unknown
 Unknown
 RNY4P6,TAGLN,PRR13P3,RN7SL828P,SCN2B,HSPE1P18,CD3G,TTC36,RPL5P30,RNU6-1157P,MIR6716,TREHP1,RNU6-376P,SETP16,CXCR5,MIR4492,RPL23AP64,RPS25,TRAPPC4,HMBS,DPAGT1,PDZD3,RNU6-262P,MCAM,MIR6756,RNF26,C1QTNF5,DUXAP5,RNU6-1123P,TMEM136,ELOCP22,HMGB1P42,RPS4XP12,BMPR1AP2,RNU6-256P,MIR125B1,BLID,MIRLET7A2,MIR100,RNU4ATAC10P,RNU4ATAC5P,RNU6-592P,GLULP3,RNU4-23P,ATP5PBP5,RPL34P23,RPS26P43,RPL31P47,SNORD14E,SNORD14D,SNORD14C,PHBP17,MIR4493,SF3A3P2,OR6X1,RNU1-21P,OR6M1,OR6M2P,OR6M3P,TMEM225,OR8D4,OR4D5,OR6T1,OR10G6,OR10G5P,OR10G4,OR10G9,OR10G7,OR10D5P,OR10D4P,OR10D1P,OR10D3,OR8F1P,OR8G3P,OR8G2P,OR8G7P,OR8G1,OR8G5,SLC5A4P1,OR8D2,OR8B7P,OR8B6P,OR8B5P,OR8B1P,OR8C1P,OR8B2,OR8B3,OR8X1P,OR8B4,OR8B8,OR8A2P,OR8B9P,OR8B10P,OR8A3P,OR8B12,OR8Q1P,RNA5SP352,NRGN,ESAM,HEPN1,PKNOX2-AS1,RNU6-321P,RNU6-1156P,RNU2-35P,ACRV1,PATE2,PATE3,PATE4,VSIG10L2,NAP1L1P1,RNU4-86P,RN7SL351P,SRPRA,RPL35AP26,MIR3167,KIRREL3-AS3,RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,APOA1-AS,PAFAH1B2,SIDT2,PCSK7,RNF214,BACE1-AS,CEP164,FXYD2,FXYD6,TMPRSS13,IL10RA,SMIM35,SCN4B,JAML,MPZL2,CD3E,CD3D,UBE4A,ATP5MG,TMEM25,IFT46,ARCN1,TREH,BCL9L,UPK2,RN7SL688P,FOXR1,SLC37A4,HYOU1,VPS11,H2AFX,C2CD2L,HINFP,ABCG4,NLRX1,CCDC153,MFRP,USP2,THY1,KRT8P7,TRIM29,OAF,POU2F3,TBCEL,SC5D,CRTAM,BSX,HSPA8,SCN3B,OR10S1,OR10G8,OR10N1P,OR8D1,OR8A1,PANX3,TBRG1,SPA17,VSIG2,ROBO3,ROBO4,HEPACAM,CCDC15,SLC37A2,TMEM218,KRT18P59,EI24,STT3A,CHEK1,PATE1,HYLS1,PUS3,DDX25,RPUSD4,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3-AS1,KIRREL3-AS2,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,SIK3,BACE1,FXYD6-FXYD2,TMPRSS4,MPZL3,PHLDB1,DDX6,CCDC84,CBL,USP2-AS1,NECTIN1,ARHGEF12,TECTA,SORL1,MIR100HG,JHY,CLMP,GRAMD1B,VWA5A,SIAE,PKNOX2,FEZ1,CDON,FAM118B,GSEC,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,KMT2A,GRIK4,UBASH3B,ZNF202,MSANTD2,KIRREL3,ARHGAP32,NTM,OPCML,DSCAML1,NCAPD3
 
 kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00000903
 FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
 
 Unknown
 Unknown
 Unknown
 DUXAP5,RNU6-1123P,TMEM136,ELOCP22,HMGB1P42,RPS4XP12,BMPR1AP2,RNU6-256P,MIR125B1,BLID,MIRLET7A2,MIR100,RNU4ATAC10P,RNU4ATAC5P,RNU6-592P,GLULP3,RNU4-23P,ATP5PBP5,RPL34P23,RPS26P43,RPL31P47,SNORD14E,SNORD14D,SNORD14C,PHBP17,MIR4493,SF3A3P2,OR6X1,RNU1-21P,OR6M1,OR6M2P,OR6M3P,TMEM225,OR8D4,OR4D5,OR6T1,OR10G6,OR10G5P,OR10G4,OR10G9,OR10G7,OR10D5P,OR10D4P,OR10D1P,OR10D3,OR8F1P,OR8G3P,OR8G2P,OR8G7P,OR8G1,OR8G5,SLC5A4P1,OR8D2,OR8B7P,OR8B6P,OR8B5P,OR8B1P,OR8C1P,OR8B2,OR8B3,OR8X1P,OR8B4,OR8B8,OR8A2P,OR8B9P,OR8B10P,OR8A3P,OR8B12,OR8Q1P,RNA5SP352,NRGN,ESAM,HEPN1,PKNOX2-AS1,RNU6-321P,RNU6-1156P,RNU2-35P,ACRV1,PATE2,PATE3,PATE4,VSIG10L2,NAP1L1P1,RNU4-86P,RN7SL351P,SRPRA,RPL35AP26,MIR3167,KIRREL3-AS3,RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,KRT8P7,TRIM29,OAF,POU2F3,TBCEL,SC5D,CRTAM,BSX,HSPA8,SCN3B,OR10S1,OR10G8,OR10N1P,OR8D1,OR8A1,PANX3,TBRG1,SPA17,VSIG2,ROBO3,ROBO4,HEPACAM,CCDC15,SLC37A2,TMEM218,KRT18P59,EI24,STT3A,CHEK1,PATE1,HYLS1,PUS3,DDX25,RPUSD4,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3-AS1,KIRREL3-AS2,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,USP2-AS1,NECTIN1,ARHGEF12,TECTA,SORL1,MIR100HG,JHY,CLMP,GRAMD1B,VWA5A,SIAE,PKNOX2,FEZ1,CDON,FAM118B,GSEC,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,GRIK4,UBASH3B,ZNF202,MSANTD2,KIRREL3,ARHGAP32,NTM,OPCML,NCAPD3
 
 kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00001146
 FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
 
 Unknown
 Unknown
 Unknown
 SETP16,CXCR5,MIR4492,RPL23AP64,RPS25,TRAPPC4,HMBS,DPAGT1,PDZD3,RNU6-262P,MCAM,MIR6756,RNF26,C1QTNF5,DUXAP5,RNU6-1123P,TMEM136,ELOCP22,HMGB1P42,RPS4XP12,BMPR1AP2,RNU6-256P,MIR125B1,BLID,MIRLET7A2,MIR100,RNU4ATAC10P,RNU4ATAC5P,RNU6-592P,GLULP3,RNU4-23P,ATP5PBP5,RPL34P23,RPS26P43,RPL31P47,SNORD14E,SNORD14D,SNORD14C,PHBP17,MIR4493,SF3A3P2,OR6X1,RNU1-21P,OR6M1,OR6M2P,OR6M3P,TMEM225,OR8D4,OR4D5,OR6T1,OR10G6,OR10G5P,OR10G4,OR10G9,OR10G7,OR10D5P,OR10D4P,OR10D1P,OR10D3,OR8F1P,OR8G3P,OR8G2P,OR8G7P,OR8G1,OR8G5,SLC5A4P1,OR8D2,OR8B7P,OR8B6P,OR8B5P,OR8B1P,OR8C1P,OR8B2,OR8B3,OR8X1P,OR8B4,OR8B8,OR8A2P,OR8B9P,OR8B10P,OR8A3P,OR8B12,OR8Q1P,RNA5SP352,NRGN,ESAM,HEPN1,PKNOX2-AS1,RNU6-321P,RNU6-1156P,RNU2-35P,ACRV1,PATE2,PATE3,PATE4,VSIG10L2,NAP1L1P1,RNU4-86P,RN7SL351P,SRPRA,RPL35AP26,MIR3167,KIRREL3-AS3,RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,BCL9L,UPK2,RN7SL688P,FOXR1,SLC37A4,HYOU1,VPS11,H2AFX,C2CD2L,HINFP,ABCG4,NLRX1,CCDC153,MFRP,USP2,THY1,KRT8P7,TRIM29,OAF,POU2F3,TBCEL,SC5D,CRTAM,BSX,HSPA8,SCN3B,OR10S1,OR10G8,OR10N1P,OR8D1,OR8A1,PANX3,TBRG1,SPA17,VSIG2,ROBO3,ROBO4,HEPACAM,CCDC15,SLC37A2,TMEM218,KRT18P59,EI24,STT3A,CHEK1,PATE1,HYLS1,PUS3,DDX25,RPUSD4,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3-AS1,KIRREL3-AS2,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,DDX6,CCDC84,CBL,USP2-AS1,NECTIN1,ARHGEF12,TECTA,SORL1,MIR100HG,JHY,CLMP,GRAMD1B,VWA5A,SIAE,PKNOX2,FEZ1,CDON,FAM118B,GSEC,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,GRIK4,UBASH3B,ZNF202,MSANTD2,KIRREL3,ARHGAP32,NTM,OPCML,NCAPD3
 
 kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004178
 FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
 
 Unknown
 Unknown
 Unknown
 TMEM136,ELOCP22,HMGB1P42,RPS4XP12,BMPR1AP2,RNU6-256P,MIR125B1,BLID,MIRLET7A2,MIR100,RNU4ATAC10P,RNU4ATAC5P,RNU6-592P,GLULP3,RNU4-23P,ATP5PBP5,RPL34P23,RPS26P43,RPL31P47,SNORD14E,SNORD14D,SNORD14C,PHBP17,MIR4493,SF3A3P2,OR6X1,RNU1-21P,OR6M1,OR6M2P,OR6M3P,TMEM225,OR8D4,OR4D5,OR6T1,OR10G6,OR10G5P,OR10G4,OR10G9,OR10G7,OR10D5P,OR10D4P,OR10D1P,OR10D3,OR8F1P,OR8G3P,OR8G2P,OR8G7P,OR8G1,OR8G5,SLC5A4P1,OR8D2,OR8B7P,OR8B6P,OR8B5P,OR8B1P,OR8C1P,OR8B2,OR8B3,OR8X1P,OR8B4,OR8B8,OR8A2P,OR8B9P,OR8B10P,OR8A3P,OR8B12,OR8Q1P,RNA5SP352,NRGN,ESAM,HEPN1,PKNOX2-AS1,RNU6-321P,RNU6-1156P,RNU2-35P,ACRV1,PATE2,PATE3,PATE4,VSIG10L2,NAP1L1P1,RNU4-86P,RN7SL351P,SRPRA,RPL35AP26,MIR3167,KIRREL3-AS3,RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,POU2F3,TBCEL,SC5D,CRTAM,BSX,HSPA8,SCN3B,OR10S1,OR10G8,OR10N1P,OR8D1,OR8A1,PANX3,TBRG1,SPA17,VSIG2,ROBO3,ROBO4,HEPACAM,CCDC15,SLC37A2,TMEM218,KRT18P59,EI24,STT3A,CHEK1,PATE1,HYLS1,PUS3,DDX25,RPUSD4,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3-AS1,KIRREL3-AS2,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,ARHGEF12,TECTA,SORL1,MIR100HG,JHY,CLMP,GRAMD1B,VWA5A,SIAE,PKNOX2,FEZ1,CDON,FAM118B,GSEC,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,GRIK4,UBASH3B,ZNF202,MSANTD2,KIRREL3,ARHGAP32,NTM,OPCML,NCAPD3
 
 kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004549
 FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
 
 Unknown
 Unknown
 Unknown
 RNU6-262P,MCAM,MIR6756,RNF26,C1QTNF5,DUXAP5,RNU6-1123P,TMEM136,ELOCP22,HMGB1P42,RPS4XP12,BMPR1AP2,RNU6-256P,MIR125B1,BLID,MIRLET7A2,MIR100,RNU4ATAC10P,RNU4ATAC5P,RNU6-592P,GLULP3,RNU4-23P,ATP5PBP5,RPL34P23,RPS26P43,RPL31P47,SNORD14E,SNORD14D,SNORD14C,PHBP17,MIR4493,SF3A3P2,OR6X1,RNU1-21P,OR6M1,OR6M2P,OR6M3P,TMEM225,OR8D4,OR4D5,OR6T1,OR10G6,OR10G5P,OR10G4,OR10G9,OR10G7,OR10D5P,OR10D4P,OR10D1P,OR10D3,OR8F1P,OR8G3P,OR8G2P,OR8G7P,OR8G1,OR8G5,SLC5A4P1,OR8D2,OR8B7P,OR8B6P,OR8B5P,OR8B1P,OR8C1P,OR8B2,OR8B3,OR8X1P,OR8B4,OR8B8,OR8A2P,OR8B9P,OR8B10P,OR8A3P,OR8B12,OR8Q1P,RNA5SP352,NRGN,ESAM,HEPN1,PKNOX2-AS1,RNU6-321P,RNU6-1156P,RNU2-35P,ACRV1,PATE2,PATE3,PATE4,VSIG10L2,NAP1L1P1,RNU4-86P,RN7SL351P,SRPRA,RPL35AP26,MIR3167,KIRREL3-AS3,RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,MFRP,USP2,THY1,KRT8P7,TRIM29,OAF,POU2F3,TBCEL,SC5D,CRTAM,BSX,HSPA8,SCN3B,OR10S1,OR10G8,OR10N1P,OR8D1,OR8A1,PANX3,TBRG1,SPA17,VSIG2,ROBO3,ROBO4,HEPACAM,CCDC15,SLC37A2,TMEM218,KRT18P59,EI24,STT3A,CHEK1,PATE1,HYLS1,PUS3,DDX25,RPUSD4,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3-AS1,KIRREL3-AS2,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,CBL,USP2-AS1,NECTIN1,ARHGEF12,TECTA,SORL1,MIR100HG,JHY,CLMP,GRAMD1B,VWA5A,SIAE,PKNOX2,FEZ1,CDON,FAM118B,GSEC,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,GRIK4,UBASH3B,ZNF202,MSANTD2,KIRREL3,ARHGAP32,NTM,OPCML,NCAPD3
 
 kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004702
 FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
 
 Unknown
 Unknown
 Unknown
 ELOCP22,HMGB1P42,RPS4XP12,BMPR1AP2,RNU6-256P,MIR125B1,BLID,MIRLET7A2,MIR100,RNU4ATAC10P,RNU4ATAC5P,RNU6-592P,GLULP3,RNU4-23P,ATP5PBP5,RPL34P23,RPS26P43,RPL31P47,SNORD14E,SNORD14D,SNORD14C,PHBP17,MIR4493,SF3A3P2,OR6X1,RNU1-21P,OR6M1,OR6M2P,OR6M3P,TMEM225,OR8D4,OR4D5,OR6T1,OR10G6,OR10G5P,OR10G4,OR10G9,OR10G7,OR10D5P,OR10D4P,OR10D1P,OR10D3,OR8F1P,OR8G3P,OR8G2P,OR8G7P,OR8G1,OR8G5,SLC5A4P1,OR8D2,OR8B7P,OR8B6P,OR8B5P,OR8B1P,OR8C1P,OR8B2,OR8B3,OR8X1P,OR8B4,OR8B8,OR8A2P,OR8B9P,OR8B10P,OR8A3P,OR8B12,OR8Q1P,RNA5SP352,NRGN,ESAM,HEPN1,PKNOX2-AS1,RNU6-321P,RNU6-1156P,RNU2-35P,ACRV1,PATE2,PATE3,PATE4,VSIG10L2,NAP1L1P1,RNU4-86P,RN7SL351P,SRPRA,RPL35AP26,MIR3167,KIRREL3-AS3,RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,TBCEL,SC5D,CRTAM,BSX,HSPA8,SCN3B,OR10S1,OR10G8,OR10N1P,OR8D1,OR8A1,PANX3,TBRG1,SPA17,VSIG2,ROBO3,ROBO4,HEPACAM,CCDC15,SLC37A2,TMEM218,KRT18P59,EI24,STT3A,CHEK1,PATE1,HYLS1,PUS3,DDX25,RPUSD4,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3-AS1,KIRREL3-AS2,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,TECTA,SORL1,MIR100HG,JHY,CLMP,GRAMD1B,VWA5A,SIAE,PKNOX2,FEZ1,CDON,FAM118B,GSEC,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,GRIK4,UBASH3B,ZNF202,MSANTD2,KIRREL3,ARHGAP32,NTM,OPCML,NCAPD3
 
 kushima_18_SCZ_discovery_cases-caseSCZ0616
 While a subset of CNVs were reported to have been validated by qPCR in the report, precisely which CNVs were validated was not reported
 
 Unknown
 Unknown
 Unknown
 RPL23AP64,RPS25,TRAPPC4,HMBS,DPAGT1,PDZD3,RNU6-262P,MCAM,MIR6756,RNF26,C1QTNF5,DUXAP5,RNU6-1123P,TMEM136,ELOCP22,HMGB1P42,RPS4XP12,BMPR1AP2,RNU6-256P,MIR125B1,BLID,MIRLET7A2,MIR100,RNU4ATAC10P,RNU4ATAC5P,RNU6-592P,GLULP3,RNU4-23P,ATP5PBP5,RPL34P23,RPS26P43,RPL31P47,SNORD14E,SNORD14D,SNORD14C,PHBP17,MIR4493,SF3A3P2,OR6X1,RNU1-21P,OR6M1,OR6M2P,OR6M3P,TMEM225,OR8D4,OR4D5,OR6T1,OR10G6,OR10G5P,OR10G4,OR10G9,OR10G7,OR10D5P,OR10D4P,OR10D1P,OR10D3,OR8F1P,OR8G3P,OR8G2P,OR8G7P,OR8G1,OR8G5,SLC5A4P1,OR8D2,OR8B7P,OR8B6P,OR8B5P,OR8B1P,OR8C1P,OR8B2,OR8B3,OR8X1P,OR8B4,OR8B8,OR8A2P,OR8B9P,OR8B10P,OR8A3P,OR8B12,OR8Q1P,RNA5SP352,NRGN,ESAM,HEPN1,PKNOX2-AS1,RNU6-321P,RNU6-1156P,RNU2-35P,ACRV1,PATE2,PATE3,PATE4,VSIG10L2,NAP1L1P1,RNU4-86P,RN7SL351P,SRPRA,RPL35AP26,MIR3167,KIRREL3-AS3,RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,SLC37A4,HYOU1,VPS11,H2AFX,C2CD2L,HINFP,ABCG4,NLRX1,CCDC153,MFRP,USP2,THY1,KRT8P7,TRIM29,OAF,POU2F3,TBCEL,SC5D,CRTAM,BSX,HSPA8,SCN3B,OR10S1,OR10G8,OR10N1P,OR8D1,OR8A1,PANX3,TBRG1,SPA17,VSIG2,ROBO3,ROBO4,HEPACAM,CCDC15,SLC37A2,TMEM218,KRT18P59,EI24,STT3A,CHEK1,PATE1,HYLS1,PUS3,DDX25,RPUSD4,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3-AS1,KIRREL3-AS2,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,CCDC84,CBL,USP2-AS1,NECTIN1,ARHGEF12,TECTA,SORL1,MIR100HG,JHY,CLMP,GRAMD1B,VWA5A,SIAE,PKNOX2,FEZ1,CDON,FAM118B,GSEC,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,GRIK4,UBASH3B,ZNF202,MSANTD2,KIRREL3,ARHGAP32,NTM,OPCML,NCAPD3
 
 tzetis_12_DD/ID_discovery_cases-case31
 
 
 Unknown
 Unknown
 
 ELOCP22,HMGB1P42,RPS4XP12,BMPR1AP2,RNU6-256P,MIR125B1,BLID,MIRLET7A2,MIR100,RNU4ATAC10P,RNU4ATAC5P,RNU6-592P,GLULP3,RNU4-23P,ATP5PBP5,RPL34P23,RPS26P43,RPL31P47,SNORD14E,SNORD14D,SNORD14C,PHBP17,MIR4493,SF3A3P2,OR6X1,RNU1-21P,OR6M1,OR6M2P,OR6M3P,TMEM225,OR8D4,OR4D5,OR6T1,OR10G6,OR10G5P,OR10G4,OR10G9,OR10G7,OR10D5P,OR10D4P,OR10D1P,OR10D3,OR8F1P,OR8G3P,OR8G2P,OR8G7P,OR8G1,OR8G5,SLC5A4P1,OR8D2,OR8B7P,OR8B6P,OR8B5P,OR8B1P,OR8C1P,OR8B2,OR8B3,OR8X1P,OR8B4,OR8B8,OR8A2P,OR8B9P,OR8B10P,OR8A3P,OR8B12,OR8Q1P,RNA5SP352,NRGN,ESAM,HEPN1,PKNOX2-AS1,RNU6-321P,RNU6-1156P,RNU2-35P,ACRV1,PATE2,PATE3,PATE4,VSIG10L2,NAP1L1P1,RNU4-86P,RN7SL351P,SRPRA,RPL35AP26,MIR3167,KIRREL3-AS3,RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,TBCEL,SC5D,CRTAM,BSX,HSPA8,SCN3B,OR10S1,OR10G8,OR10N1P,OR8D1,OR8A1,PANX3,TBRG1,SPA17,VSIG2,ROBO3,ROBO4,HEPACAM,CCDC15,SLC37A2,TMEM218,KRT18P59,EI24,STT3A,CHEK1,PATE1,HYLS1,PUS3,DDX25,RPUSD4,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3-AS1,KIRREL3-AS2,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,ARHGEF12,TECTA,SORL1,MIR100HG,JHY,CLMP,GRAMD1B,VWA5A,SIAE,PKNOX2,FEZ1,CDON,FAM118B,GSEC,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,GRIK4,UBASH3B,ZNF202,MSANTD2,KIRREL3,ARHGAP32,NTM,OPCML,NCAPD3
 

Controls

No Control Data Available
No Animal Model Data Available
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