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12p12.2CNV Type: Deletion-Duplication


Largest CNV size: 107993 bp

Statistics Box:
Number of Reports: 10



Summary Information

Summary statement in development

Additional Locus Information

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USCS Symbol             NCBI Symbol

Decipher

            Decipher Symbol

References

Major Reports

Title
Author, Year
Report Class
CNV Type
Functional impact of global rare copy number variation in autism spectrum disorders.
Deletion
Excess of rare, inherited truncating mutations in autism.
Deletion-Duplication
Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder
Deletion

Minor Reports

Title
Author, Year
Report Class
CNV Type
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Deletion-Duplication
Rare de novo and transmitted copy-number variation in autistic spectrum disorders.
Deletion
Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder.
Deletion
Performance of case-control rare copy number variation annotation in classification of autism.
Deletion
NA
Duplication
NA
Deletion
NA
Duplication

Cases

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 engchuan_15_ASD_discovery_cases
 Samples from the Autism Genome Project (AGP)
 1892
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 N/A
 85.78% Male
 34261
 2
 0
 2
 han_22_ASD/DD/ID_discovery_cases
  NA NA
 Probands with ASD or unexplained developmental delay/intellectual disability with or without other congenital anomalies from Shandong province in Northern China who were referred for genetic services from January 2014 to December 2018.
 410
 151 cases diagnosed with ASD (DSM-5 criteria, ADOS-2, confirmed by CARS score > 30) and 259 patients diagnosed with developmental delay/intellectual disability (DSM-5 criteria, confirmed by Gesell developmental scale DQ score < 75 and Wechsler Intelligence Scale for Children-Revised with IQ<70).
 Mean age, 2 yrs. 11 mos.
 68.78% Male
 41772
 0
 1
 1
 krumm_15_ASD_discovery_cases
 Probands from the Simons Simplex Collection
 2377
 Diagnosis of ASD
 N/A
 N/A
 65148
 7
 1
 8
 kushima_22_SCZ_discovery_cases
 Japanese schizophrenia probands evaluated for copy number variation from an initial cohort of 3,111 probands before quality control.
 3014
 Cases diagnosed with schizophrenia (SCZ) according to DSM-5 criteria.
 Median age, 45 yrs.
 53.5% Male
 20338
 1
 0
 1
 larson_17_ASD_discovery_cases
  NA NA
 Participants with a dual diagnosis of ASD and psychosis that were recruited from clinical services in the public and independent sectors in the United Kingdom, as well as from charities and an Asperger's syndrome social networking website (study took place from January 2011 and April 2014)
 116
 All cases with a dual diagnosis of ASD and psychosis (affective, schizophrenic, and atypical)
 N/A
 N/A
 24010
 0
 1
 1
 levy_11_ASD_discovery_cases
 Autistic probands from 887 families from the Simons Simplex Collection (SSC)
 858
 ASD
 
 87.06% Male
 106993
 1
 0
 1
 pinto_10_ASD_discovery_cases
 Autism Genome Project (AGP) consortium patient cohort from families with at least two ASD individuals
 996
 ASD (ADI-R and ADOS): strict, broad, or spectrum ASD
 
 
 32405
 1
 0
 1
 poultney_13_ASD_discovery_cases
 ASD cases of European ancestry from AGRE retained after filtering (original cohort size of 432 cases)
 299
 Cases diagnosed with ASD
 N/A
 79.86% Male (before filtering)
 8372
 1
 0
 1
 sanders_11_ASD_discovery_cases
 Autistic probands from the Simons Simplex Collection (SSC). 872 probands in quartet families, 272 probands in trios.
 1124
 ASD diagnosis: 89.5% autism; 8.5% PDD-NOS, 2% Asperger syndrome. Mean full-scale IQ 85.1 1.5 (mean verbal IQ, 81.9 1.7; mean non-verbal IQ, 88.4 1.4)
 Mean, 9.1 yrs.
 86.1% Male
 107993
 9
 1
 10
 stamouli_18_ASD/NDD_discovery_cases
  NA NA
 Affected individuals from 100 twin pairs (69 monozygotic, 31 dizygotic), corresponding to 97 families, that were enriched for neurodevelopmental disorders from the Roots of Autism and ADHD Study in Sweden (RATSS)
 100 twin pairs
 Diagnoses based on DSM-5 criteria following evaluation using standard diagnostic tools [a psychosocial and anamnestic interview, the Autism Diagnosis Interview-Revised (ADI-R), the Autism Diagnostic Observation Schedule Second Edition (ADOS-2), the Kiddie Schedule for Affective Disorders and Schizophrenia (K-SADS), or the Diagnostic Interview for ADHD in Adults (DIVA)]; Wechsler Intelligence Scale for Children or Adults, Fourth Edition (WISC-IV) or the Leiter-revised scales in combination with the Peabody Picture Vocabulary Test, Third Edition, and the parent-based Adaptive Behavior Assessment Scale, 2nd Edition (ABAS-2) were also used to evaluate adaptive, cognitive, and verbal abilities an
 N/A
 N/A
 120278
 2
 0
 2

Controls

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 bacchelli_20_ASD_discovery_controls
  NA NA
 Anonymized DNA samples from Italian individuals with no psychiatric disorders
 365
 Control
 N/A
 54.52% Male
 11695
 1
 0
 1
 engchuan_15_ASD_discovery_controls
 Platform-matched controls from three large studies: SAGE (Study of Addiction Genetics and Environment), Ontario Colorectal Cancer study, and HABC (Health Aging and Body Composition)
 2342
 Controls; subjects had no previous psychiatric history
 N/A
 46.67% Male
 67376
 1
 1
 2
 krumm_15_ASD_discovery_controls
 Unaffected siblings from quad families from the Simons Simplex Collection
 1786
 Control
 N/A
 N/A
 61222
 5
 1
 6
 kushima_22_ASD/BPD/SCZ_discovery_controls
 Psychiatrically normal control individuals selected from the general population evaluated for copy number variation from an initial cohort of 2,713 control individuals before quality control.
 2671
 Controls were psychiatrically normal and had no history of mental disorders based on responses to questionnaires or self-reporting.
 Median age, 36 yrs.
 47.8% Male
 0
 0
 0
 0
 larson_17_ASD_discovery_controls
  NA NA
 Entries listed in the Database of Genomic Variants (up to October 2017)
 N/A
 Control
 N/A
 N/A
 24010
 0
 1
 1
 levy_11_ASD_discovery_controls
 Unaffected siblings of autistic probands from 887 families from the Simons Simplex Collection (SSC)
 863
 Control
 
 47.97% Male
 0
 0
 0
 0
 nord_11_ASD_discovery_controls
 Samples from 367 total control individuals (319 European American, 48 African American) used to test for differences in rare CNV prevalence compared with autism cases
 123
 Controls (no history of psychiatric symptoms by self-report)
 30 yrs.
 
 46434
 1
 0
 1
 poultney_13_ASD_discovery_controls
 Controls matched for European ancestry from NIMH and CEPH retained after filtering (original cohort size of 379 controls)
 260
 Control
 N/A
 47.49% Male (before filtering)
 20851
 2
 0
 2
 sanders_11_ASD_discovery_controls
 Matched siblings of autistic probands from the Simons Simplex Collection (SSC).
 872
 Controls
 Mean, 10.0 yrs.
 
 408695
 5
 0
 5

Cases

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
 engchuan_15_ASD_discovery_cases
  Caucasian
 Solid phase hybridization
  Illumina 1M
 
 
 None
 han_22_ASD/DD/ID_discovery_cases
  Han Chinese
 Array SNP
  Affymetrix SNP 6.0, Affymetrix CytoScan HD
 
 
 
 krumm_15_ASD_discovery_cases
  N/A
 WES
 
 CoNIFER, XHMM
 
 Solid phase hybridization (Illumina 1M, 1 M Duo, or Omni 2.5)
 kushima_22_SCZ_discovery_cases
  Japan
 aCGH
  NimbleGen 720K Whole-Genome Tiling, Agilent SurePrint G3 Human CGH 400K
 Fast Adaptive States Segmentation Technique 2
 BioDiscovery Nexus Copy Number v.9.0
 qRT-PCR
 larson_17_ASD_discovery_cases
  United Kingdom
 Array SNP
  Affymetrix CytoScan HD 2.8M, Affymetrix Cytogenetics
 SNP-FASST2 Segmentation
 Nexus Copy Number 7 (BioDiscovery), Affymetrix ChAS
 None
 levy_11_ASD_discovery_cases
 
 aCGH
  NimbleGen HD2
 HMM
 
 
 pinto_10_ASD_discovery_cases
  European
 Solid phase hybridization
  Illumina Infinium 1M SNP microarray
 QuantiSNP, iPattern
 
 qPCR, long-range PCR (LR-PCR), MLPA, FISH, aCGH (Agilent 1M), array SNP (Affymetrix 500K)
 poultney_13_ASD_discovery_cases
  European
 WES
  Agilent SureSelect Human All Exon v.2
 XHMM
 
 None
 sanders_11_ASD_discovery_cases
  White non-Hispanic, 74.5%; mixed, 9.3%, Asian, 4.3%, White Hispanic, 4.0%, African-American, 3.8%; other, 4.2&
 Solid phase hybridization
  Illumina 1M v1, Illumina 1M v3
 PennCNV, QuantiSNP, GNOSIS
 
 
 stamouli_18_ASD/NDD_discovery_cases
  Swedish
 Solid phase hybridization
  Illumina Infinium PsychArray-24 v1.1
 PennCNV, QuantiSNP, iPattern, iPsychCNV
 
 None

Controls

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
  bacchelli_20_ASD_discovery_controls
  Italian
  Solid phase hybridization
  Illumina Infinium PsychArray
  PennCNV, QuantiSNP, CNVPartition
 
  None
  engchuan_15_ASD_discovery_controls
  Caucasian
  Solid phase hybridization
  Illumina 1M
 
 
  None
  krumm_15_ASD_discovery_controls
  N/A
  WES
 
  CoNIFER, XHMM
 
  Solid phase hybridization (Illumina 1M, 1 M Duo, or Omni 2.5)
  kushima_22_ASD/BPD/SCZ_discovery_controls
  Japan
  aCGH
  NimbleGen 720K Whole-Genome Tiling, Agilent SurePrint G3 Human CGH 400K
  Fast Adaptive States Segmentation Technique 2
  BioDiscovery Nexus Copy Number v.9.0
  qRT-PCR
  larson_17_ASD_discovery_controls
  N/A
  N/A
  N/A
 
 
 
  levy_11_ASD_discovery_controls
 
  aCGH
  NimbleGen HD2
  HMM
 
 
  nord_11_ASD_discovery_controls
 
  aCGH
  NimbleGen HD2
  Sliding-window algorithm, ~10 kb minumum size threshold
 
  None
  poultney_13_ASD_discovery_controls
  European
  WES
  Agilent SureSelect Human All Exon v.2
  XHMM
 
  None
  sanders_11_ASD_discovery_controls
 
  Solid phase hybridization
  Illumina 1M v1 or Illumina 1M v3
  PennCNV, QuantiSNP, GNOSIS
 
 

Cases

Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
  engchuan_15_ASD_discovery_cases-case13046_553
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 20571418
 20605679
  34262
 GRCh38
 Deletion
 No
  engchuan_15_ASD_discovery_cases-case5112_4
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 20888700
 20921104
  32405
 GRCh38
 Deletion
 No
  han_22_ASD/DD/ID_discovery_cases-caseY108
  NA NA
 4 yrs. 7 mos.
 M
 ASD
 
 
 20845153
 20886924
  41772
 GRCh38
 Duplication
 No
  krumm_15_ASD_discovery_cases-case11285.p1
 N/A
 Male
 ASD
 Proband from the Simons Simplex Collection (SSC). Family type: Quad
 
 20862755
 20883604
  20850
 GRCh38
 Deletion
 Yes
  krumm_15_ASD_discovery_cases-case11329.p1
 N/A
 Male
 ASD
 Proband from the Simons Simplex Collection (SSC). Family type: Trio
 
 20875234
 20883604
  8371
 GRCh38
 Deletion
 Yes
  krumm_15_ASD_discovery_cases-case12382.p1
 N/A
 Male
 ASD
 Proband from the Simons Simplex Collection (SSC). Family type: Quad
 
 20750674
 20815822
  65149
 GRCh38
 Deletion
 Yes
  krumm_15_ASD_discovery_cases-case12655.p1
 N/A
 Male
 ASD
 Proband from the Simons Simplex Collection (SSC). Family type: Quad
 
 20875234
 20883604
  8371
 GRCh38
 Deletion
 Yes
  krumm_15_ASD_discovery_cases-case13134.p1
 N/A
 Male
 ASD
 Proband from the Simons Simplex Collection (SSC). Family type: Trio
 
 20875234
 20883602
  8369
 GRCh38
 Deletion
 Yes
  krumm_15_ASD_discovery_cases-case13864.p1
 N/A
 Male
 ASD
 Proband from the Simons Simplex Collection (SSC). Family type: Quad
 
 20858438
 20862856
  4419
 GRCh38
 Deletion
 Yes
  krumm_15_ASD_discovery_cases-case14181.p1
 N/A
 Male
 ASD
 Proband from the Simons Simplex Collection (SSC). Family type: Quad
 
 20855027
 20916249
  61223
 GRCh38
 Duplication
 Yes
  krumm_15_ASD_discovery_cases-case14272.p1
 N/A
 Male
 ASD
 Proband from the Simons Simplex Collection (SSC). Family type: Quad
 
 20875234
 20883604
  8371
 GRCh38
 Deletion
 Yes
  kushima_22_SCZ_discovery_cases-caseSCZ2385
 NA
 NA
 Schizophrenia
 Diagnosis of schizophrenia according to DSM-5 criteria.
 
 20857217
 20877554
  20338
 GRCh38
 Deletion
 Yes
  larson_17_ASD_discovery_cases-case86
  NA NA
 N/A
 N/A
 ASD and psychosis
 No additional clinical information available. Patient carries CNV that is present in DGV (less than 1.5%) but was not present in 1124 ASD cases without psychosis from the Simons Simplex Collection.
 
 20417636
 20441646
  24011
 GRCh38
 Duplication
 No
  levy_11_ASD_discovery_cases-12382.p1
 NA
 M
 ASD
 NA
 NA
 20746569
 20853561
  106993
 GRCh38
 Deletion
 No
  pinto_10_ASD_discovery_cases-case5112_4
 NA
 M
 ASD
 NA
 NA
 20888700
 20921104
  32405
 GRCh38
 Deletion
 Yes
  poultney_13_ASD_discovery_cases-case98HI0371B
 N/A
 M
 ASD
 ASD case from AGRE (AGRE ID AU032804; NDAR ID N/A)
 
 20875233
 20883604
  8372
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-11107.p1
 6.9
 M
 Autism
 NA
 Full-scale IQ, 30; non-verbal IQ, 37; verbal IQ, 25
 20915248
 20929342
  14095
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-11285.p1
 15.3
 M
 Autism
 NA
 Full-scale IQ, 13; non-verbal IQ, 20; verbal IQ, 5
 20865197
 20886215
  21019
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-11329.p1
 8.7
 M
 Autism
 NA
 Full-scale IQ, 104; non-verbal IQ, 105; verbal IQ, 103
 20865197
 20883599
  18403
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-11370.p1
 14.6
 M
 Autism
 NA
 Full-scale IQ, 100; non-verbal IQ, 110; verbal IQ 102
 20434258
 20501634
  67377
 GRCh38
 Duplication
 No
  sanders_11_ASD_discovery_cases-11391.p1
 15.2
 M
 Autism
 NA
 Full-scale IQ, 116; non-verbal IQ, 116; verbal IQ, 113
 20862205
 20883599
  21395
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-11556.p1
 9.7
 M
 Autism
 NA
 Full-scale IQ, 102; non-verbal IQ, 102; verbal IQ, 108
 20184251
 20186007
  1757
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-12382.p1
 10.1
 M
 Autism
 NA
 Full-scale IQ, 91; non-verbal IQ, 94; verbal IQ, 88
 20745188
 20853181
  107994
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-12382.p1
 10.1
 M
 Autism
 NA
 Full-scale IQ, 91; non-verbal IQ, 94; verbal IQ, 88
 20728828
 20734057
  5230
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-12449.p1
 6.8
 M
 Autism
 NA
 Full-scale IQ, 87; non-verbal IQ, 87; verbal IQ, 93
 20184251
 20186007
  1757
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-12655.p1
 8.9
 M
 Autism
 NA
 Full-scale IQ, 48; non-verbal IQ, 64; verbal IQ, 28
 20864354
 20883599
  19246
 GRCh38
 Deletion
 No
  stamouli_18_ASD/NDD_discovery_cases-family5_Twin_1
  NA NA
 N/A
 N/A
 ASD/NDD
 Case is from a monozygotic twin pair from the Discordant ASD/Concordant NDD diagnostic group
 
 20732904
 20853181
  120278
 GRCh38
 Deletion
 No
  stamouli_18_ASD/NDD_discovery_cases-family5_Twin_2
  NA NA
 N/A
 N/A
 ASD/NDD
 Case is from a monozygotic twin pair from the Discordant ASD/Concordant NDD diagnostic group
 
 20732904
 20853181
  120278
 GRCh38
 Deletion
 No

Controls

Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
  bacchelli_20_ASD_discovery_controls-control20054
  N/A
  F
  Control
  Control
 
  20871905
  20883599
  11695
  GRCh38
  Deletion
  No
  engchuan_15_ASD_discovery_controls-control110036015782_
  N/A
  N/A
  Control
  No previous psychiatric history
 
  20434258
  20501634
  67377
  GRCh38
  Duplication
  No
  engchuan_15_ASD_discovery_controls-controlB850068_1007871741
  N/A
  N/A
  Control
  No previous psychiatric history
 
  20888700
  20921104
  32405
  GRCh38
  Deletion
  No
  krumm_15_ASD_discovery_controls-control11285.s1
  N/A
  Male
  Control
  Unaffected sibling from the Simons Simplex Collection (SSC)
 
  20875234
  20883604
  8371
  GRCh38
  Deletion
  Yes
  krumm_15_ASD_discovery_controls-control13072.s1
  N/A
  Female
  Control
  Unaffected sibling from the Simons Simplex Collection (SSC)
 
  20875234
  20883604
  8371
  GRCh38
  Deletion
  Yes
  krumm_15_ASD_discovery_controls-control13129.s1
  N/A
  Female
  Control
  Unaffected sibling from the Simons Simplex Collection (SSC)
 
  20875234
  20883604
  8371
  GRCh38
  Deletion
  Yes
  krumm_15_ASD_discovery_controls-control13855.s1
  N/A
  Female
  Control
  Unaffected sibling from the Simons Simplex Collection (SSC)
 
  20875234
  20883604
  8371
  GRCh38
  Deletion
  Yes
  krumm_15_ASD_discovery_controls-control14181.s1
  N/A
  Female
  Control
  Unaffected sibling from the Simons Simplex Collection (SSC)
 
  20855027
  20916249
  61223
  GRCh38
  Duplication
  Yes
  krumm_15_ASD_discovery_controls-control14272.s1
  N/A
  Female
  Control
  Unaffected sibling from the Simons Simplex Collection (SSC)
 
  20875234
  20883604
  8371
  GRCh38
  Deletion
  Yes
  nord_11_ASD_discovery_controls-04C27935
 
 
  Control
 
 
  19958300
  20004733
  46434
  Unknown
  Deletion
 
  poultney_13_ASD_discovery_controls-control04C27734A
  N/A
  F
  Control
  NIMH Control (NIMH ID 28812)
 
  20862754
  20883604
  20851
  GRCh38
  Deletion
  No
  poultney_13_ASD_discovery_controls-control04C31231A
  N/A
  M
  Control
  NIMH Control (NIMH ID 33455)
 
  20875233
  20883604
  8372
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-11107.s1
  3.7
  M
  Control (matched sibling)
  NA
  NA
  20915248
  20933449
  18202
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-11285.s1
  16.4
  M
  Control (matched sibling)
  NA
  NA
  20865197
  20883599
  18403
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-11329.s1
  6.9
  M
  Control (matched sibling)
  NA
  NA
  20862676
  20883599
  20924
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-11753.s1
  15.1
  F
  Control (matched sibling)
  NA
  NA
  20864354
  20884619
  20266
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-13072.s1
  8.7
  F
  Control (matched sibling)
  NA
  NA
  20864354
  20883599
  19246
  GRCh38
  Deletion
  No

Cases

Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
 engchuan_15_ASD_discovery_cases-case13046_553
 
 
 Unknown
 
 
 PDE3A
 
 engchuan_15_ASD_discovery_cases-case5112_4
 
 
 Unknown
 
 
 SLCO1B3
 
 han_22_ASD/DD/ID_discovery_cases-caseY108
 
 
 Unknown
 
 
 SLCO1B3,SLCO1B3-SLCO1B7
 
 krumm_15_ASD_discovery_cases-case11285.p1
 Illumina 1M
 
 Paternal
 Simplex
 Not segregated (CNV in unaffected sibling)
 SLCO1B3
 
 krumm_15_ASD_discovery_cases-case11329.p1
 Illumina 1M
 
 Maternal
 Simplex
 Segregated
 SLCO1B3
 
 krumm_15_ASD_discovery_cases-case12382.p1
 Illumina 1MDuo
 
 Paternal
 Simplex
 Segregated
 SLCO1C1,SLCO1B3
 
 krumm_15_ASD_discovery_cases-case12655.p1
 Illumina 1MDuo
 
 Paternal
 Simplex
 Segregated
 SLCO1B3
 
 krumm_15_ASD_discovery_cases-case13134.p1
 1M-Duov3
 
 Paternal
 Simplex
 Segregated
 SLCO1B3
 
 krumm_15_ASD_discovery_cases-case13864.p1
 Omni2.5-4v1
 
 Paternal
 Simplex
 Segregated
 SLCO1B3
 
 krumm_15_ASD_discovery_cases-case14181.p1
 Omni2.5-4v1
 
 Maternal
 Simplex
 Not segregated (CNV in unaffected sibling)
 SLCO1B3
 
 krumm_15_ASD_discovery_cases-case14272.p1
 Omni2.5-4v1
 
 Paternal
 Simplex
 Not segregated (CNV in unaffected sibling)
 SLCO1B3
 
 kushima_22_SCZ_discovery_cases-caseSCZ2385
 qRT-PCR
 
 Unknown
 
 
 SLCO1B3,SLCO1B3-SLCO1B7
 
 larson_17_ASD_discovery_cases-case86
 
 
 Unknown
 
 Unknown
 PDE3A
 
 levy_11_ASD_discovery_cases-12382.p1
 
 
 Paternal
 Simplex
 Segregated
 SLCO1C1,SLCO1B3
 
 pinto_10_ASD_discovery_cases-case5112_4
 Agilent1M
 
 paternal
 NA
 NA
 SLCO1B3
 
 poultney_13_ASD_discovery_cases-case98HI0371B
 
 
 Unknown
 Unknown (likely multiplex/AGRE)
 Unknown
 SLCO1B3
 
 sanders_11_ASD_discovery_cases-11107.p1
 
 
 Paternal
 Simplex (quad-proband matched)
 Not segregated
 SLCO1B3
 
 sanders_11_ASD_discovery_cases-11285.p1
 
 
 Paternal
 Simplex (quad-proband matched)
 Not segregated
 SLCO1B3
 
 sanders_11_ASD_discovery_cases-11329.p1
 
 
 Maternal
 Simplex (quad-proband matched)
 Not segregated
 SLCO1B3
 
 sanders_11_ASD_discovery_cases-11370.p1
 
 
 Paternal
 Simplex (trio)
 NA
 UBE2L2,PDE3A
 
 sanders_11_ASD_discovery_cases-11391.p1
 
 
 Maternal
 Simplex (quad-proband matched)
 Not segregated
 SLCO1B3
 
 sanders_11_ASD_discovery_cases-11556.p1
 
 
 Maternal
 Simplex (quad-proband matched)
 Not segregated
 
 
 sanders_11_ASD_discovery_cases-12382.p1
 
 
 Paternal
 Simplex (quad-proband matched)
 Not segregated
 SLCO1C1,SLCO1B3
 
 sanders_11_ASD_discovery_cases-12382.p1
 
 
 Paternal
 Simplex (quad-proband matched)
 Not segregated
 SLCO1C1
 
 sanders_11_ASD_discovery_cases-12449.p1
 
 
 Paternal
 Simplex (quad-proband matched)
 Not segregated
 
 
 sanders_11_ASD_discovery_cases-12655.p1
 
 
 Paternal
 Simplex (quad-proband matched)
 Not segregated
 SLCO1B3
 
 stamouli_18_ASD/NDD_discovery_cases-family5_Twin_1
 
 
 Unknown
 Multiplex
 Segregated (CNV present in both affected twins)
 SLCO1C1,SLCO1B3
 
 stamouli_18_ASD/NDD_discovery_cases-family5_Twin_2
 
 
 Unknown
 Multiplex
 Segregated (CNV present in both affected twins)
 SLCO1C1,SLCO1B3
 

Controls

Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
bacchelli_20_ASD_discovery_controls-control20054
 
 
  Unknown
 
 
  SLCO1B3,SLCO1B3-SLCO1B7
 
engchuan_15_ASD_discovery_controls-control110036015782_
 
 
  Unknown
 
 
  UBE2L2,PDE3A
 
engchuan_15_ASD_discovery_controls-controlB850068_1007871741
 
 
  Unknown
 
 
  SLCO1B3
 
krumm_15_ASD_discovery_controls-control11285.s1
  Illumina 1M
 
  Paternal
 
 
  SLCO1B3
 
krumm_15_ASD_discovery_controls-control13072.s1
  Illumina 1MDuo
 
  Paternal
 
 
  SLCO1B3
 
krumm_15_ASD_discovery_controls-control13129.s1
  1M-Duov3
 
  Maternal
 
 
  SLCO1B3
 
krumm_15_ASD_discovery_controls-control13855.s1
  Omni2.5-4v1
 
  Maternal
 
 
  SLCO1B3
 
krumm_15_ASD_discovery_controls-control14181.s1
  Omni2.5-4v1
 
  Maternal
 
 
  SLCO1B3
 
krumm_15_ASD_discovery_controls-control14272.s1
  Omni2.5-4v1
 
  Paternal
 
 
  SLCO1B3
 
nord_11_ASD_discovery_controls-04C27935
 
 
 
 
 
  0 genes
 
poultney_13_ASD_discovery_controls-control04C27734A
 
 
  Unknown
 
 
  SLCO1B3
 
poultney_13_ASD_discovery_controls-control04C31231A
 
 
  Unknown
 
 
  SLCO1B3
 
sanders_11_ASD_discovery_controls-11107.s1
 
 
  Paternal
  Simplex (quad)
  NA
  SLCO1B3
 
sanders_11_ASD_discovery_controls-11285.s1
 
 
  Paternal
  Simplex (quad)
  NA
  SLCO1B3
 
sanders_11_ASD_discovery_controls-11329.s1
 
 
  Maternal
  Simplex (quad)
  NA
  SLCO1B3
 
sanders_11_ASD_discovery_controls-11753.s1
 
 
  Maternal
  Simplex (quad)
  NA
  SLCO1B3
 
sanders_11_ASD_discovery_controls-13072.s1
 
 
  Paternal
  Simplex (quad)
  NA
  SLCO1B3
 

No Animal Model Data Available
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