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9q33.2CNV Type: Deletion-Duplication


Largest CNV size: 188987 bp

Statistics Box:
Number of Reports: 10



Summary Information

Summary statement in development

Additional Locus Information

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USCS Symbol             NCBI Symbol

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            Decipher Symbol

References

Major Reports

Title
Author, Year
Report Class
CNV Type
Functional impact of global rare copy number variation in autism spectrum disorders.
Duplication
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabili...
Deletion
Excess of rare, inherited truncating mutations in autism.
Duplication

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
A discovery resource of rare copy number variations in individuals with autism spectrum disorder.
Duplication
Transmission disequilibrium of small CNVs in simplex autism.
Duplication
Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder.
Duplication
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.
Duplication
Performance of case-control rare copy number variation annotation in classification of autism.
Deletion-Duplication
The landscape of copy number variations in Finnish families with autism spectrum disorders.
Deletion

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
 188986
 1
 3
 4
 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
 2531624
 1
 0
 1
 kanduri_15_ASD_discovery_cases
 Autistic cases from an initial sample of 83 Finnish families comprising 257 family members following quality control
 80
 Diagnosis of ASD based on DSM-IV, 4th edition, or ICD-10 criteria; patients screened based on Childhood Autism Rating Scale (CARS), Asperger Syndrome Screening Questionnaire, and Asperger's Syndrome Diagnostic Interview.
 N/A
 N/A
 209656
 1
 0
 1
 krumm_13_ASD_discovery_cases
 Probands from quad families ascertained as part of the Simons Simplex Collection (SSC); CNVs detected using data from four previously published exome sequencing studies (O'Roak et al., 2011; Iossifov et al., 2012; O'Roak et al., 2012; Sanders et al., 2012)
 411
 Diagnosis of ASD. Social Responsiveness Scale (SRS) used as a quantitative measure of social deficits
 N/A
 81.265% Male
 26665
 0
 1
 1
 krumm_15_ASD_discovery_cases
 Probands from the Simons Simplex Collection
 2377
 Diagnosis of ASD
 N/A
 N/A
 42642
 0
 1
 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
 
 
 188987
 0
 2
 2
 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)
 239986
 0
 1
 1
 prasad_12_ASD_discovery_cases
 Unrelated ASD cases recruited from three Canadian sites (Hospital for Sick Children, McMaster University, and Memorial University of Newfoundland); the majority of cases had been previously genotyped with results published in Marshall et al., 2008 and Pinto et al., 2010. 20 cases from initial cohort of 696 were excluded from further analysis (due to CNVs > 5 Mb).
 676
 Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS
 NA
 82.84% Male
 23212
 0
 2
 2
 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
 48699
 2
 1
 3
 woodbury-smith_14_ASD_discovery_cases
 Probands from 19 extended ASD pedigrees (defined as at least three ASD cases spread across at least two nuclear families); 6 families recruited in Canada, 13 families recruited in the United States
 19
 Diagnosis of ASD made using combination of ADI-R, ADOS, and clinical judgment in conjunction with DSM-IV criteria.
 N/A
 N/A
 45686
 0
 1
 1

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
 147393
 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
 91560
 0
 2
 2
 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
 kanduri_15_ASD_discovery_controls
 Unrelated Finnish samples from the cohort of Health 2000 survey from an initial sample of 288 individuals following quality control
 269
 Controls screened for DSM-IV mental disorders using the Composite International Diagnostic Interview and psychotic disorders using the research version of the Structured Clinical Interview for DSM-IV
 N/A
 N/A
 0
 0
 0
 0
 krumm_13_ASD_discovery_controls
 Unaffected siblings of ASD probands from quad families ascertained as part of the Simons Simplex Collection (SSC); CNVs detected using data from four previously published exome sequencing studies (O'Roak et al., 2011; Iossifov et al., 2012; O'Roak et al., 2012; Sanders et al., 2012)
 411
 Control (unaffected siblings of ASD probands). Social Responsiveness Scale (SRS) used as a quantitative measure of social deficits
 N/A
 46.47% Male
 26665
 1
 1
 2
 krumm_15_ASD_discovery_controls
 Unaffected siblings from quad families from the Simons Simplex Collection
 1786
 Control
 N/A
 N/A
 23214
 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)
 349334
 0
 4
 4
 prasad_12_ASD_discovery_controls
 PDx controls [1000 DNA samples from reportedly healthy donors (50.2% male) from BioServe (Beltsville, MD)] and 4139 in-house controls previously reported in Krawcak et al. 2006, Stewart et al. 2009, and Bierut et al. 2010. CNVs identified in controls were used to define rare ASD-specific CNVs.
 5139
 Control
 NA
 NA (PDx controls 50.2% male)
 23212
 0
 0
 0
 sanders_11_ASD_discovery_controls
 Matched siblings of autistic probands from the Simons Simplex Collection (SSC).
 872
 Controls
 Mean, 10.0 yrs.
 
 23068
 3
 0
 3
 woodbury-smith_14_ASD_discovery_controls
 Platform-matched controls from the KORA and COGEND datasets
 2988
 Control
 N/A
 N/A
 0
 0
 0
 0

Cases

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
 engchuan_15_ASD_discovery_cases
  Caucasian
 Solid phase hybridization
  Illumina 1M
 
 
 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
 kanduri_15_ASD_discovery_cases
  Finnish
 Solid phase hybridization
  Illumina Human OmniExpress-12v1.0 BeadChip
 QuantiSNP, PennCNV
 Illumina BeadStudio
 None
 krumm_13_ASD_discovery_cases
  N/A
 WES
  Whole exome sequencing platforms used in four recent publications (O'Roak et al., 2011; Sanders et al., 2012; O'Roak et al., 2012, and Iossifov et al., 2012)
 DNACopy, CGHCall
 CoNIFER
 None
 krumm_15_ASD_discovery_cases
  N/A
 WES
 
 CoNIFER, XHMM
 
 Solid phase hybridization (Illumina 1M, 1 M Duo, or Omni 2.5)
 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
 prasad_12_ASD_discovery_cases
  Canada
 aCGH
  Agilent 1M
 ADM-2, DNAcopy (R Bioconductor)
 DNA Analytics v4.0.85 (Agilent), DNAcopy
 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
 
 
 woodbury-smith_14_ASD_discovery_cases
  US and Canada
 Solid phase hybridization
  Illumina HumanOmni2.5 BeadChip
 
 PennCNV, QuantiSNP, iPattern
 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
  kaminsky_11_DD/ID/ASD_discovery_controls
  NA
  aCGH
  Agilent 44K, Agilent 105K
 
  Feature Extraction, DNA Analytics
 
  kanduri_15_ASD_discovery_controls
  Finnish
  Solid phase hybridization
  Illumina Infinium HD Human610-Quad BeadChip
  QuantiSNP, PennCNV
  Illumina BeadStudio
  None
  krumm_13_ASD_discovery_controls
  N/A
  WES
  Whole exome sequencing platforms used in four recent publications (O'Roak et al., 2011; Sanders et al., 2012; O'Roak et al., 2012, and Iossifov et al., 2012)
  DNACopy, CGHCall
  CoNIFER
  Solid phase hybridization (Illumina 1M), aCGH (Agilent SurePrint G3 4x180K), or confirmed by manual inspection
  krumm_15_ASD_discovery_controls
  N/A
  WES
 
  CoNIFER, XHMM
 
  Solid phase hybridization (Illumina 1M, 1 M Duo, or Omni 2.5)
  poultney_13_ASD_discovery_controls
  European
  WES
  Agilent SureSelect Human All Exon v.2
  XHMM
 
  None
  prasad_12_ASD_discovery_controls
  NA
  aCGH
  Agilent 1M
  ADM-2, DNAcopy (R Bioconductor)
  DNA Analytics v4.0.85 (Agilent), DNAcopy
 
  sanders_11_ASD_discovery_controls
 
  Solid phase hybridization
  Illumina 1M v1 or Illumina 1M v3
  PennCNV, QuantiSNP, GNOSIS
 
 
  woodbury-smith_14_ASD_discovery_controls
  Predominantly European
  Solid phase hybridization
  Illumina HumanOmni2.5 BeadChip
 
  PennCNV, QuantiSNP, iPattern
  None

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-case14111_2000
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 122407651
 122596637
  188987
 GRCh38
 Duplication
 No
  engchuan_15_ASD_discovery_cases-case14184_3020
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 122407651
 122596637
  188987
 GRCh38
 Duplication
 No
  engchuan_15_ASD_discovery_cases-case14329_4430
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 122415212
 122589027
  173816
 GRCh38
 Duplication
 No
  engchuan_15_ASD_discovery_cases-case4420_1
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 122601929
 122681766
  79838
 GRCh38
 Deletion
 No
  kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004982
 NA
 NA
 Developmental delay/intellectual disability/ASD
 Clinical profile NA
 Cognitive profile NA
 120938041
 123469664
  2531624
 GRCh38
 Deletion
 Yes
  kanduri_15_ASD_discovery_cases-case2923
 N/A
 N/A
 ASD
 Diagnosis of ASD based on DSM-IV, 4th edition, or ICD-10 criteria; patient screened based on Childhood Autism Rating Scale (CARS), Asperger Syndrome Screening Questionnaire, and/or Asperger's Syndrome Diagnostic Interview.
 
 122623813
 122833468
  209656
 Unknown
 Deletion
 No
  krumm_13_ASD_discovery_cases-case13296.p1
 N/A
 M
 ASD
 ASD proband from SSC quad family 13296. SRS score of 87.
 Full-scale IQ (FSIQ) score of 30.
 122800122
 122826787
  26666
 GRCh38
 Duplication
 No (not tested)
  krumm_15_ASD_discovery_cases-case12539.p1
 N/A
 Male
 ASD
 Proband from the Simons Simplex Collection (SSC). Family type: Trio
 
 122823015
 122865657
  42643
 GRCh38
 Duplication
 Yes
  pinto_10_ASD_discovery_cases-case14111_2000
 NA
 M
 Autism
 Mild asphyxia during delivery, did not require reanimation; no language delay, neurodevelopmental delay at 2 y, no epilepsy, no dysmorphic features
 Normal IQ
 122407651
 122596637
  188987
 GRCh38
 Duplication
 Yes
  pinto_10_ASD_discovery_cases-case14184_3020
 NA
 M
 ASD
 No language delay, no epilepsy, no dysmorphic features
 Normal IQ
 122407651
 122596637
  188987
 GRCh38
 Duplication
 Yes
  poultney_13_ASD_discovery_cases-case00HI1663A
 N/A
 F
 ASD
 ASD case from AGRE (AGRE ID AU056708; NDAR ID NDAR_INVAC801FDF)
 
 122510800
 122750785
  239986
 GRCh38
 Duplication
 No
  prasad_12_ASD_discovery_cases-case107433
 NA
 M
 ASD
 Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS. Novel CNV
 
 123451254
 123460804
  9551
 Unknown
 Duplication
 No
  prasad_12_ASD_discovery_cases-case80186
 NA
 M
 ASD
 Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS. Novel CNV
 
 123751383
 123774594
  23212
 Unknown
 Duplication
 No
  sanders_11_ASD_discovery_cases-12539.p1
 7.9
 M
 Autism
 NA
 Full-scale IQ, 106; non-verbal IQ, 108; verbal IQ, 104
 122823630
 122872329
  48700
 GRCh38
 Duplication
 No
  sanders_11_ASD_discovery_cases-12661.p1
 8.4
 F
 Autism
 NA
 Full-scale IQ, 48; non-verbal IQ, 59; verbal IQ, 33
 122391073
 122392631
  1559
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-12796.p1
 5.2
 M
 Autism
 NA
 Full-scale IQ, 68; non-verbal IQ, 72; verbal IQ, 68
 121035046
 121046826
  11781
 GRCh38
 Deletion
 No
  woodbury-smith_14_ASD_discovery_cases-case10
 N/A
 M
 ASD
 Family history: broad autism phenotype (BAP)-defined father.
 
 122823630
 122869315
  45686
 GRCh38
 Duplication
 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-control10078
  N/A
  F
  Control
  Control
 
  121312363
  121459755
  147393
  GRCh38
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlB479722_1007875261
  N/A
  N/A
  Control
  No previous psychiatric history
 
  121247816
  121298986
  51171
  GRCh38
  Duplication
  No
  engchuan_15_ASD_discovery_controls-controlB763762_1007874874
  N/A
  N/A
  Control
  No previous psychiatric history
 
  122553754
  122645314
  91561
  GRCh38
  Duplication
  No
  krumm_13_ASD_discovery_controls-control11437.s1
  N/A
  M
  Control
  Unaffected sibling from SSC quad family 11437. SRS score of 35.
 
  121135805
  121159019
  23215
  GRCh38
  Deletion
  No (not tested)
  krumm_13_ASD_discovery_controls-control13296.s1
  N/A
  F
  Control
  Unaffected sibling from SSC quad family 13296. SRS score of 40.
 
  122800122
  122826787
  26666
  GRCh38
  Duplication
  Yes
  krumm_15_ASD_discovery_controls-control11437.s1
  N/A
  Male
  Control
  Unaffected sibling from the Simons Simplex Collection (SSC)
 
  121135805
  121159019
  23215
  GRCh38
  Deletion
  Yes
  poultney_13_ASD_discovery_controls-control04C31170A
  N/A
  F
  Control
  NIMH Control (NIMH ID 59702)
 
  120415038
  120612539
  197502
  GRCh38
  Duplication
  No
  poultney_13_ASD_discovery_controls-control04C31170A
  N/A
  F
  Control
  NIMH Control (NIMH ID 59702)
 
  120961480
  121008500
  47021
  GRCh38
  Duplication
  No
  poultney_13_ASD_discovery_controls-control05C44621
  N/A
  M
  Control
  NIMH Control (NIMH ID 39000)
 
  120411356
  120608010
  196655
  GRCh38
  Duplication
  No
  poultney_13_ASD_discovery_controls-control05C44621
  N/A
  M
  Control
  NIMH Control (NIMH ID 39000)
 
  122510800
  122860133
  349334
  GRCh38
  Duplication
  No
  sanders_11_ASD_discovery_controls-11437.s1
  18.4
  M
  Control (matched sibling)
  NA
  NA
  121135217
  121158285
  23069
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-12858.s1
  6.3
  F
  Control (matched sibling)
  NA
  NA
  121217503
  121236064
  18562
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-13015.s1
  7.1
  F
  Control (matched sibling)
  NA
  NA
  122389961
  122393651
  3691
  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-case14111_2000
 
 
 Unknown
 
 
 OR1J1,OR1J2,OR1N1,OR1N2,OR1J4,OR1L8
 
 engchuan_15_ASD_discovery_cases-case14184_3020
 
 
 Unknown
 
 
 OR1J1,OR1J2,OR1N1,OR1N2,OR1J4,OR1L8
 
 engchuan_15_ASD_discovery_cases-case14329_4430
 
 
 Unknown
 
 
 OR1J1,OR1J2,OR1N1,OR1N2,OR1J4,OR1L8
 
 engchuan_15_ASD_discovery_cases-case4420_1
 
 
 Unknown
 
 
 OR1H1P,OR1Q1,OR1B1,OR1L1,OR1L3
 
 kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004982
 FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
 
 Unknown
 Unknown
 Unknown
 RN7SL181P,GSN-AS1,RN7SL187P,MIR4478,OR1J1,OR1J2,OR1N1,OR1N2,OR1H1P,OR1Q1,OR1B1,OR1L1,OR1L3,TLK1P1,OR1L4,SKA2P1,OR5C1,OR1K1,KRT18P67,SNORD90,RNY1P15,GPR21,MIR600HG,MIR600,MIR601,RAB14,STOM,GGTA1P,HMGB1P37,MORN5,LHX6,RBM18,PTGS1,OR1J4,OR1L8,OR1L6,RC3H2,ZBTB6,ZBTB26,CRB2,C5,CNTRL,GSN,TTLL11,TTLL11-IT1,NDUFA8,MRRF,PDCL,RABGAP1,STRBP,DAB2IP,DENND1A
 
 kanduri_15_ASD_discovery_cases-case2923
 
 
 Paternal
 Unknown
 Unknown
 Intergenic CNV: nearest genes, BRINP1(dist=492074),MIR147A(dist=173789)
 
 krumm_13_ASD_discovery_cases-case13296.p1
 
 
 Maternal
 Simplex
 Not segregated
 OR1K1,PDCL
 
 krumm_15_ASD_discovery_cases-case12539.p1
 Illumina 1MDuo
 
 Maternal
 Simplex
 Segregated
 KRT18P67,RC3H2,PDCL
 
 pinto_10_ASD_discovery_cases-case14111_2000
 qPCR-Paternal
 
 paternal
 Simplex
 NA
 OR1J1,OR1J2,OR1N1,OR1N2,OR1J4,OR1L8
 
 pinto_10_ASD_discovery_cases-case14184_3020
 qPCR-Maternal
 
 maternal
 Simplex
 NA
 OR1J1,OR1J2,OR1N1,OR1N2,OR1J4,OR1L8
 
 poultney_13_ASD_discovery_cases-case00HI1663A
 
 
 Unknown
 Unknown (likely multiplex/AGRE)
 Unknown
 OR1J2,OR1N1,OR1N2,OR1H1P,OR1Q1,OR1B1,OR1L1,OR1L3,TLK1P1,OR1L4,OR1J4,OR1L8,OR1L6
 
 prasad_12_ASD_discovery_cases-case107433
 
 
 Unknown
 Unknown
 Unknown
 MIR548D1,DAB2IP,MIR548AA1
 
 prasad_12_ASD_discovery_cases-case80186
 
 
 Unknown
 Unknown
 Unknown
 TTLL11,MIR548D1,MIR548AA1
 
 sanders_11_ASD_discovery_cases-12539.p1
 
 
 Maternal
 Simplex (trio)
 NA
 KRT18P67,RC3H2,PDCL
 
 sanders_11_ASD_discovery_cases-12661.p1
 
 
 Unknown
 Simplex (quad-proband matched)
 Segregated
 PTGS1
 
 sanders_11_ASD_discovery_cases-12796.p1
 
 
 Unknown
 Simplex (quad-proband matched)
 Not segregated
 C5
 
 woodbury-smith_14_ASD_discovery_cases-case10
 
 
 Paternal
 Possible multi-generational (CNV transmitted from BAP-defined parent to ASD diagnosed offspring)
 Unknown
 KRT18P67,RC3H2,PDCL
 

Controls

Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
bacchelli_20_ASD_discovery_controls-control10078
 
 
  Unknown
 
 
  STOM,GGTA1P,GSN
 
engchuan_15_ASD_discovery_controls-controlB479722_1007875261
 
 
  Unknown
 
 
  GSN-AS1,GSN
 
engchuan_15_ASD_discovery_controls-controlB763762_1007874874
 
 
  Unknown
 
 
  OR1N2,OR1H1P,OR1Q1,OR1B1,OR1L8
 
krumm_13_ASD_discovery_controls-control11437.s1
 
 
  Paternal
  Simplex
 
  CNTRL
 
krumm_13_ASD_discovery_controls-control13296.s1
  aCGH (Agilent SurePrint G3 4x180K)
 
  Maternal
  Simplex
 
  OR1K1,PDCL
 
krumm_15_ASD_discovery_controls-control11437.s1
  Illumina 1M
 
  Paternal
 
 
  CNTRL
 
poultney_13_ASD_discovery_controls-control04C31170A
 
 
  Unknown
 
 
  MEGF9,CDK5RAP2
 
poultney_13_ASD_discovery_controls-control04C31170A
 
 
  Unknown
 
 
  C5
 
poultney_13_ASD_discovery_controls-control05C44621
 
 
  Unknown
 
 
  MEGF9,CDK5RAP2
 
poultney_13_ASD_discovery_controls-control05C44621
 
 
  Unknown
 
 
  OR1J2,OR1N1,OR1N2,OR1H1P,OR1Q1,OR1B1,OR1L1,OR1L3,TLK1P1,OR1L4,SKA2P1,OR5C1,OR1K1,KRT18P67,OR1J4,OR1L8,OR1L6,RC3H2,PDCL
 
sanders_11_ASD_discovery_controls-11437.s1
 
 
  Paternal
  Simplex (quad)
  NA
  CNTRL
 
sanders_11_ASD_discovery_controls-12858.s1
 
 
  Paternal
  Simplex (quad)
  NA
  RAB14,GSN
 
sanders_11_ASD_discovery_controls-13015.s1
 
 
  Unknown
  Simplex (quad)
  NA
  PTGS1
 

No Animal Model Data Available
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