9p22.3CNV Type: Deletion-Duplication
Largest CNV size: 287035 bp
Statistics Box:
Number of Reports: 11
Number of Reports: 11
Summary Information
Summary statement in development
Additional Locus Information
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
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
No Animal Model Data Available


