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9p22.3CNV Type: Deletion-Duplication


Largest CNV size: 287035 bp

Statistics Box:
Number of Reports: 11



Summary Information

Summary statement in development

Additional Locus Information

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USCS Symbol             NCBI Symbol

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References

Major Reports

Title
Author, Year
Report Class
CNV Type
Structural variation of chromosomes in autism spectrum disorder.
Duplication
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabili...
Deletion
A discovery resource of rare copy number variations in individuals with autism spectrum disorder.
Deletion
Excess of rare, inherited truncating mutations in autism.
Duplication

Minor Reports

Title
Author, Year
Report Class
CNV Type
Rare structural variation of synapse and neurotransmission genes in autism.
Deletion
Reduced transcript expression of genes affected by inherited and de novo CNVs in autism.
Deletion
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Deletion-Duplication
Transmission disequilibrium of small CNVs in simplex autism.
Deletion-Duplication
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-Duplication
Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder.
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
 83629
 2
 1
 3
 gai_11_ASD_replication_cases
 Replication case samples derived from AGRE sets 1-3
 593
 Idiopathic autism; cases designated as 'spectrum' and 'not quite autism' excluded, as were cases with known genetic syndromes or other non-idiopathic causes
 
 
 118705
 2
 0
 2
 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
 1106694
 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
 59325
 1
 1
 2
 krumm_15_ASD_discovery_cases
 Probands from the Simons Simplex Collection
 2377
 Diagnosis of ASD
 N/A
 N/A
 11425
 0
 1
 1
 marshall_08_ASD_discovery_cases
 Cohort of ASD families (237 simplex, 189 mulitplex) recruited from the Hospital for Sick Children, McMaster Univ., Memorial Univ., and other sites
 427
 ASD
 
 
 287035
 0
 1
 1
 nord_11_ASD_discovery_cases
 Youth with ASD (as part of mother-father-child trios)
 41
 ASD
 
 85.4% Male
 9930
 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)
 53998
 1
 0
 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
 21729
 2
 0
 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
 76443
 4
 1
 5
 yin_16_ASD_discovery_cases
 Discovery cohort of ASD cases recruited from the Department of Psychiatry of National Taiwan University Hospital (NTUH), Chang Gung Memorial Hospital (CGMH), Taoyuan, and Taoyuan Mental Hospital (TMH), Taiwan.
 335
 Cases diagnosed with autistic disorder according to DSM-IV and confirmed by using the Chinese version of ADI-R. Cases' autistic behaviors assessed by Social Responsiveness Scale (SRS), and cognitive functions assessed by the Weschler Intelligence Scale for Children-Third Edition (WISC-III) and the Wisconsin Card Sorting Test (WCST).
 Mean, 9.39 4.04 yrs.
 89.3% Male
 2144
 0
 1
 1

Controls

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 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
 114137
 5
 2
 7
 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
 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
 0
 0
 0
 0
 krumm_15_ASD_discovery_controls
 Unaffected siblings from quad families from the Simons Simplex Collection
 1786
 Control
 N/A
 N/A
 0
 0
 0
 0
 marshall_08_ASD_discovery_controls_1
 German PopGen project and entries from Database of Genomic Variants
 500
 Controls
 
 
 0
 0
 0
 0
 marshall_08_ASD_discovery_controls_2
 Non-disease controls from Ontario population
 1152
 Controls
 
 
 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.
 
 0
 0
 0
 0
 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)
 12064
 0
 1
 1
 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)
 21729
 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.
 
 16381
 4
 0
 4
 yin_16_ASD_discovery_controls
 Individuals from the Han Chinese Cell and Genome Bank (HCCGB) in Taiwan
 1093
 Controls
 Mean, 68.07 10.12 yrs.
 48.0% Male
 2144
 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
 gai_11_ASD_replication_cases
  European
 Solid phase hybridization
  Illumina Infinium II HumanHap550 BeadChip
 
 BeadStudio 3.0
 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
 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)
 marshall_08_ASD_discovery_cases
  90% European, 4.5% European-mixed, 4.5% Asian, 0.07% African
 Array SNP, karotyping
  Affymetrix 500K
 dChip, CNAG, GEMCA
 
 qPCR, qmPCR
 nord_11_ASD_discovery_cases
  29 European American, 3 Asian American, 2 Hispanic, 2 African American, 5 unknown ancestry
 aCGH
  NimbleGen HD2
 Sliding-window algorithm, ~10 kb minumum size threshold
 
 None
 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
 qPCR
 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
 
 
 yin_16_ASD_discovery_cases
  Han Chinese
 Array SNP
  Affymetrix 6.0
 
 Affymetrix Genotyping Console v.4.1
 None

Controls

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
  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
 
  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
  None
  krumm_15_ASD_discovery_controls
  N/A
  WES
 
  CoNIFER, XHMM
 
  None
  marshall_08_ASD_discovery_controls_1
  European
  Array SNP, karotyping
  Affymetrix 500K
  dChip, CNAG, GEMCA
 
 
  marshall_08_ASD_discovery_controls_2
  European
  Array SNP, karotyping
  Affymetrix 500K
  dChip, CNAG, GEMCA
 
 
  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
  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
 
 
  yin_16_ASD_discovery_controls
  Han Chinese
  Array SNP
  Affymetrix 6.0
 
  Affymetrix Genotyping Console v.4.1
  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-case16090_1571122001
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 15342233
 15405746
  63514
 GRCh38
 Duplication
 No
  engchuan_15_ASD_discovery_cases-case20112_1536001
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 15297030
 15380659
  83630
 GRCh38
 Deletion
 No
  engchuan_15_ASD_discovery_cases-case3490_3
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 16009324
 16087905
  78582
 GRCh38
 Deletion
 No
  gai_11_ASD_replication_cases-AU0941301
 
 
 Autism
 
 
 15130728
 15237714
  106987
 Unknown
 Deletion
 No
  gai_11_ASD_replication_cases-AU0941302
 
 
 Autism
 
 
 15130728
 15249432
  118705
 Unknown
 Deletion
 No
  kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00005320
 NA
 NA
 Developmental delay/intellectual disability/ASD
 Clinical profile NA
 Cognitive profile NA
 14210805
 15317500
  1106696
 GRCh38
 Deletion
 Yes
  krumm_13_ASD_discovery_cases-case12480.p1
 N/A
 M
 ASD
 ASD proband from SSC quad family 12480. SRS score of 90.
 Full-scale IQ (FSIQ) score of 86.
 15564088
 15623413
  59326
 GRCh38
 Deletion
 No (not tested)
  krumm_13_ASD_discovery_cases-case13094.p1
 N/A
 M
 ASD
 ASD proband from SSC quad family 13094. SRS score of 67.
 Full-scale IQ (FSIQ) score of 71.
 14857552
 14868977
  11426
 GRCh38
 Duplication
 No (not tested)
  krumm_15_ASD_discovery_cases-case13094.p1
 N/A
 Male
 ASD
 Proband from the Simons Simplex Collection (SSC). Family type: Quad
 
 14857552
 14868977
  11426
 GRCh38
 Duplication
 Yes
  marshall_08_ASD_discovery_cases-MM0711-003
 NA
 M
 ASD
 NA
 NA
 16102068
 16389102
  287035
 GRCh38
 Duplication
 Yes
  nord_11_ASD_discovery_cases-308-1
 
 
 ASD
 
 
 16381700
 16391629
  9930
 Unknown
 Deletion
 No
  poultney_13_ASD_discovery_cases-case03HI2532A
 N/A
 M
 ASD
 ASD case from AGRE (AGRE ID AU0941301; NDAR ID NDAR_INVUA823VB2)
 
 15172017
 15226014
  53998
 GRCh38
 Deletion
 No
  prasad_12_ASD_discovery_cases-case131240
 NA
 M
 ASD
 Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS. Novel CNV
 
 14194914
 14203254
  8341
 Unknown
 Deletion
 Yes
  prasad_12_ASD_discovery_cases-case51680
 NA
 M
 ASD
 Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS. Novel CNV
 
 15346607
 15368335
  21729
 Unknown
 Deletion
 No
  sanders_11_ASD_discovery_cases-11133.p1
 17
 M
 Autism
 NA
 Full-scale IQ, 128; non-verbal IQ, 110; verbal IQ 140
 16221345
 16222476
  1132
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-11187.p1
 7.8
 M
 Autism
 NA
 Full-scale IQ, 112; non-verbal IQ, 115; verbal IQ, 108
 16033111
 16085699
  52589
 GRCh38
 Duplication
 No
  sanders_11_ASD_discovery_cases-11841.p1
 10.4
 F
 Autism
 NA
 Full-scale IQ, 110; non-verbal IQ, 109; verbal IQ, 109
 16221345
 16222476
  1132
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-11963.p1
 6.1
 M
 ASD
 NA
 Full-scale IQ, 93; non-verbal IQ, 90; verbal IQ, 104
 15319414
 15328679
  9266
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-12480.p1
 13.1
 M
 Autism
 NA
 Full-scale IQ, 86; non-verbal IQ, 83; verbal IQ, 96
 15564906
 15641349
  76444
 GRCh38
 Deletion
 No
  yin_16_ASD_discovery_cases-case344
 N/A
 N/A
 ASD
 Cases diagnosed with autistic disorder according to DSM-IV and confirmed by using the Chinese version of ADI-R.
 
 15272232
 15274375
  2144
 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
  engchuan_15_ASD_discovery_controls-control110036010684_
  N/A
  N/A
  Control
  No previous psychiatric history
 
  15297030
  15380659
  83630
  GRCh38
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlB420588_1007854321
  N/A
  N/A
  Control
  No previous psychiatric history
 
  15426574
  15489083
  62510
  GRCh38
  Duplication
  No
  engchuan_15_ASD_discovery_controls-controlB788578_1007846129
  N/A
  N/A
  Control
  No previous psychiatric history
 
  16050349
  16085699
  35351
  GRCh38
  Duplication
  No
  engchuan_15_ASD_discovery_controls-controlHABC_900113_900113
  N/A
  N/A
  Control
  No previous psychiatric history
 
  16360891
  16391296
  30406
  GRCh38
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlHABC_900425_900425
  N/A
  N/A
  Control
  No previous psychiatric history
 
  14960219
  15037016
  76798
  GRCh38
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlHABC_902645_902645
  N/A
  N/A
  Control
  No previous psychiatric history
 
  14922879
  15037016
  114138
  GRCh38
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlHABC_902879_902879
  N/A
  N/A
  Control
  No previous psychiatric history
 
  16359610
  16391296
  31687
  GRCh38
  Deletion
  No
  poultney_13_ASD_discovery_controls-control05C41705A
  N/A
  M
  Control
  NIMH Control (NIMH ID 55192)
 
  15474007
  15486070
  12064
  GRCh38
  Duplication
  No
  sanders_11_ASD_discovery_controls-11573.s1
  10.3
  F
  Control (matched sibling)
  NA
  NA
  15319414
  15328679
  9266
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-12053.s1
  7.1
  F
  Control (matched sibling)
  NA
  NA
  15319414
  15328679
  9266
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-12534.s1
  4.7
  F
  Control (matched sibling)
  NA
  NA
  15319414
  15328679
  9266
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-12916.s1
  12.3
  M
  Control (matched sibling)
  NA
  NA
  16069318
  16085699
  16382
  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-case16090_1571122001
 
 
 Unknown
 
 
 RPL7P33
 
 engchuan_15_ASD_discovery_cases-case20112_1536001
 
 
 Unknown
 
 
 RPL7P33,TTC39B
 
 engchuan_15_ASD_discovery_cases-case3490_3
 
 
 Unknown
 
 
 CCDC171
 
 gai_11_ASD_replication_cases-AU0941301
 
 
 Inherited
 
 
 TTC39B
 
 gai_11_ASD_replication_cases-AU0941302
 
 
 Inherited
 
 
 TTC39B
 
 kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00005320
 FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
 
 De novo
 Unknown
 Unknown
 CDCA4P1,CER1,RNU6-1260P,LDHAP4,RNU6-559P,NFIB,FREM1,CLCN3P1,TTC39B,ZDHHC21
 
 krumm_13_ASD_discovery_cases-case12480.p1
 
 
 Maternal
 Simplex
 Segregated
 HMGN2P16,CCDC171
 
 krumm_13_ASD_discovery_cases-case13094.p1
 
 
 Paternal
 Simplex
 Segregated
 FREM1
 
 krumm_15_ASD_discovery_cases-case13094.p1
 1M-Duov3
 
 Paternal
 Simplex
 Segregated
 FREM1
 
 marshall_08_ASD_discovery_cases-MM0711-003
 qPCR, qmPCR
 
 Unknown
 NA
 NA
 C9orf92
 
 nord_11_ASD_discovery_cases-308-1
 
 
 Maternal
 
 
 0 genes
 
 poultney_13_ASD_discovery_cases-case03HI2532A
 
 
 Unknown
 Unknown (likely multiplex/AGRE)
 Unknown
 TTC39B
 
 prasad_12_ASD_discovery_cases-case131240
 qPCR
 
 Paternal
 Unknown
 Unknown
 NFIB
 
 prasad_12_ASD_discovery_cases-case51680
 
 
 Unknown
 Unknown
 Unknown
 0 genes
 
 sanders_11_ASD_discovery_cases-11133.p1
 
 
 Maternal
 Simplex (trio)
 NA
 C9orf92
 
 sanders_11_ASD_discovery_cases-11187.p1
 
 
 Maternal
 Simplex (quad-proband matched)
 Segregated
 CCDC171
 
 sanders_11_ASD_discovery_cases-11841.p1
 
 
 Maternal
 Simplex (trio)
 NA
 C9orf92
 
 sanders_11_ASD_discovery_cases-11963.p1
 
 
 Unknown
 Simplex (quad-proband matched)
 Not segregated
 
 
 sanders_11_ASD_discovery_cases-12480.p1
 
 
 Maternal
 Simplex (quad-proband unmatched)
 Unknown
 HMGN2P16,CCDC171
 
 yin_16_ASD_discovery_cases-case344
 
 
 Unknown
 Unknown
 Unknown
 TTC39B
 

Controls

Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
engchuan_15_ASD_discovery_controls-control110036010684_
 
 
  Unknown
 
 
  RPL7P33,TTC39B
 
engchuan_15_ASD_discovery_controls-controlB420588_1007854321
 
 
  Unknown
 
 
  RNU6-319P,SNAPC3,PSIP1
 
engchuan_15_ASD_discovery_controls-controlB788578_1007846129
 
 
  Unknown
 
 
  CCDC171
 
engchuan_15_ASD_discovery_controls-controlHABC_900113_900113
 
 
  Unknown
 
 
  C9orf92
 
engchuan_15_ASD_discovery_controls-controlHABC_900425_900425
 
 
  Unknown
 
 
  CLCN3P1
 
engchuan_15_ASD_discovery_controls-controlHABC_902645_902645
 
 
  Unknown
 
 
  CLCN3P1
 
engchuan_15_ASD_discovery_controls-controlHABC_902879_902879
 
 
  Unknown
 
 
  C9orf92
 
poultney_13_ASD_discovery_controls-control05C41705A
 
 
  Unknown
 
 
  PSIP1
 
sanders_11_ASD_discovery_controls-11573.s1
 
 
  Unknown
  Simplex (quad)
  NA
 
 
sanders_11_ASD_discovery_controls-12053.s1
 
 
  Unknown
  Simplex (quad)
  NA
 
 
sanders_11_ASD_discovery_controls-12534.s1
 
 
  Paternal
  Simplex (quad)
  NA
 
 
sanders_11_ASD_discovery_controls-12916.s1
 
 
  Paternal
  Simplex (quad)
  NA
 
 

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