9q33.2CNV Type: Deletion-Duplication
Largest CNV size: 188987 bp
Statistics Box:
Number of Reports: 10
Number of Reports: 10
Summary Information
Summary statement in development
Additional Locus Information
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
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
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


