8q24.12CNV Type: Deletion-Duplication
Largest CNV size: 47532 bp
Statistics Box:
Number of Reports: 5
Number of Reports: 5
Summary Information
Summary statement in development
Additional Locus Information
References
Major Reports
Title
Author, Year
Report Class
CNV Type
No Major Reports
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
Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation.
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
brand_15_ASD_discovery_cases
ASD cases who had been previously been screened by CNVs by CMA as part of the Simons Simplex Collection (SSC) in Sanders et al., 2011
259
Diagnosis of ASD
N/A
N/A
31815
0
2
2
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
106229
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
92739
0
1
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
47532
13
4
17
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
71595
0
2
2
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
102663
0
2
2
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
220516
1
0
1
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.
27178
1
0
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)
92739
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.
26877
6
3
9
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
71595
0
0
0
Cases
Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
brand_15_ASD_discovery_cases
N/A
Long-insert WGS
Long-insert whole genome sequencing
LUMPY, cn.MOPS, SV classifier
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
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
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
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
nord_11_ASD_discovery_controls
aCGH
NimbleGen HD2
Sliding-window algorithm, ~10 kb minumum size threshold
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
brand_15_ASD_discovery_cases-case15
N/A
N/A
ASD
Long-insert WGS identified a dupINVdup involving chromosome 8 in this case. Duplication previously identified by aCGH (chr8:122320560-122341946; hg19).
121307206
121333404
26199
GRCh38
Duplication
No
brand_15_ASD_discovery_cases-case15
N/A
N/A
ASD
Long-insert WGS identified a dupINVdup involving chromosome 8 in this case. Duplication previously identified by aCGH (chr8:122405097-122426082; hg19).
121387710
121419525
31816
GRCh38
Duplication
No
krumm_13_ASD_discovery_cases-case14110.p1
N/A
M
ASD
ASD proband from SSC quad family 14110. SRS score of 69.
Full-scale IQ (FSIQ) score of 77.
119744287
119850516
106230
GRCh38
Deletion
No (not tested)
prasad_12_ASD_discovery_cases-case93736
NA
M
ASD
Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS. CNV identified by previous SNP microarray study
121552138
121644876
92739
Unknown
Duplication
No
sanders_11_ASD_discovery_cases-11165.p1
5.2
M
Autism
NA
Full-scale IQ, 104; non-verbal IQ, 112; verbal IQ 89
118725045
118772577
47533
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11409.p1
4.1
M
Autism
NA
Full-scale IQ, 96; non-verbal IQ, 101; verbal IQ 90
119007354
119013102
5749
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11447.p1
6.6
M
Autism
NA
Full-scale IQ, 89; non-verbal IQ, 97; verbal IQ, 82
119007354
119015632
8279
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11475.p1
7.8
M
Autism
NA
Full-scale IQ, 94; non-verbal IQ, 86; verbal IQ, 110
119007354
119013102
5749
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11564.p1
10.8
M
Autism
NA
Full-scale IQ, 94; non-verbal IQ, 89; verbal IQ, 106
119007354
119013102
5749
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11794.p1
8.3
M
Autism
NA
Full-scale IQ, 36; non-verbal IQ, 40; verbal IQ, 33
119007354
119017470
10117
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11794.p1
8.3
M
Autism
NA
Full-scale IQ, 36; non-verbal IQ, 40; verbal IQ, 33
121392857
121413842
20986
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-11794.p1
8.3
M
Autism
NA
Full-scale IQ, 36; non-verbal IQ, 40; verbal IQ, 33
121308320
121329706
21387
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-11794.p1
8.3
M
Autism
NA
Full-scale IQ, 36; non-verbal IQ, 40; verbal IQ, 33
119245946
119274653
28708
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-12102.p1
5.1
M
Autism
NA
Full-scale IQ, 45; non-verbal IQ, 52; verbal IQ, 38
119007354
119015632
8279
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12221.p1
4.1
M
Autism
NA
Full-scale IQ, 89; non-verbal IQ, 99; verbal IQ, 76
119253601
119267398
13798
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-12260.p1
5.3
M
Autism
NA
Full-scale IQ, 106; non-verbal IQ, 103; verbal IQ, 109
119007354
119013102
5749
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12424.p1
4.2
M
ASD
NA
Full-scale IQ, 69; non-verbal IQ, 77; verbal IQ, 65
119007354
119013102
5749
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12717.p1
11.1
M
Autism
NA
Full-scale IQ, 89; non-verbal IQ, 94; verbal IQ, 86
119007354
119017470
10117
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12757.p1
5.3
M
Autism
NA
Full-scale IQ, 57; non-verbal IQ, 62; verbal IQ, 55
119007354
119013102
5749
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12964.p1
6.9
M
Autism
NA
Full-scale IQ, 38; non-verbal IQ, 48; verbal IQ, 28
119007354
119015632
8279
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-13013.p1
8.1
M
Autism
NA
Full-scale IQ, 72; non-verbal IQ, 68; verbal IQ, 86
119007354
119013102
5749
GRCh38
Deletion
No
yin_16_ASD_discovery_cases-case327
N/A
N/A
ASD
Cases diagnosed with autistic disorder according to DSM-IV and confirmed by using the Chinese version of ADI-R.
118576018
118577134
1117
GRCh38
Duplication
No
yin_16_ASD_discovery_cases-case328
N/A
N/A
ASD
Cases diagnosed with autistic disorder according to DSM-IV and confirmed by using the Chinese version of ADI-R.
120364045
120435638
71594
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-control110036018745_
N/A
N/A
Control
No previous psychiatric history
121314683
121417346
102664
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-control110036022051_
N/A
N/A
Control
No previous psychiatric history
121316932
121386627
69696
GRCh38
Duplication
No
krumm_13_ASD_discovery_controls-control14110.s1
N/A
F
Control
Unaffected sibling from SSC quad family 14110. SRS score of 39.
119626564
119847080
220517
GRCh38
Deletion
No (not tested)
nord_11_ASD_discovery_controls-04C27265
Control
121935857
121963034
27178
Unknown
Deletion
sanders_11_ASD_discovery_controls-11564.s1
6.3
F
Control (matched sibling)
NA
NA
119007354
119015632
8279
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-11794.s1
4.3
F
Control (matched sibling)
NA
NA
119007354
119013102
5749
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-11941.s1
8.7
F
Control (matched sibling)
NA
NA
119007354
119013102
5749
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-12220.s1
16.1
M
Control (matched sibling)
NA
NA
121308320
121335197
26878
GRCh38
Duplication
No
sanders_11_ASD_discovery_controls-12261.s1
21.5
M
Control (matched sibling)
NA
NA
119007354
119013102
5749
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-12424.s1
6.2
F
Control (matched sibling)
NA
NA
119007354
119013102
5749
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-12617.s1
14.6
M
Control (matched sibling)
NA
NA
121308320
121329706
21387
GRCh38
Duplication
No
sanders_11_ASD_discovery_controls-12617.s1
14.6
M
Control (matched sibling)
NA
NA
121392857
121417346
24490
GRCh38
Duplication
No
sanders_11_ASD_discovery_controls-13166.s1
5.6
M
Control (matched sibling)
NA
NA
119007354
119013102
5749
GRCh38
Deletion
No
Cases
Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
brand_15_ASD_discovery_cases-case15
Paternal
Simplex
Unknown
brand_15_ASD_discovery_cases-case15
Paternal
Simplex
Unknown
krumm_13_ASD_discovery_cases-case14110.p1
Paternal
Simplex
Not segregated
DSCC1,TAF2
prasad_12_ASD_discovery_cases-case93736
Unknown
Unknown
Unknown
MTBP,SNTB1
sanders_11_ASD_discovery_cases-11165.p1
Paternal
Simplex (trio)
NA
RPS26P35,SAMD12-AS1
sanders_11_ASD_discovery_cases-11409.p1
Maternal
Simplex (trio)
NA
COLEC10
sanders_11_ASD_discovery_cases-11447.p1
Paternal
Simplex (quad-proband matched)
Segregated
COLEC10
sanders_11_ASD_discovery_cases-11475.p1
Both parents
Simplex (quad-proband matched)
Segregated
COLEC10
sanders_11_ASD_discovery_cases-11564.p1
Maternal
Simplex (quad-proband matched)
Not segregated
COLEC10
sanders_11_ASD_discovery_cases-11794.p1
Both parents
Simplex (quad-proband matched)
Segregated
COLEC10
sanders_11_ASD_discovery_cases-11794.p1
Paternal
Simplex (quad-proband matched)
Not segregated
sanders_11_ASD_discovery_cases-11794.p1
Paternal
Simplex (quad-proband matched)
Not segregated
sanders_11_ASD_discovery_cases-11794.p1
Maternal
Simplex (quad-proband matched)
Segregated
MAL2-AS1
sanders_11_ASD_discovery_cases-12102.p1
Paternal
Simplex (trio)
NA
COLEC10
sanders_11_ASD_discovery_cases-12221.p1
Paternal
Simplex (quad-proband unmatched)
Unknown
sanders_11_ASD_discovery_cases-12260.p1
Maternal
Simplex (trio)
NA
COLEC10
sanders_11_ASD_discovery_cases-12424.p1
Both parents
Simplex (quad-proband matched)
Not segregated
COLEC10
sanders_11_ASD_discovery_cases-12717.p1
Maternal
Simplex (trio)
NA
COLEC10
sanders_11_ASD_discovery_cases-12757.p1
Paternal
Simplex (trio)
NA
COLEC10
sanders_11_ASD_discovery_cases-12964.p1
Paternal
Simplex (quad-proband matched)
Not segregated
COLEC10
sanders_11_ASD_discovery_cases-13013.p1
Both parents
Simplex (trio)
NA
COLEC10
yin_16_ASD_discovery_cases-case327
Unknown
Unknown
Unknown
SAMD12
yin_16_ASD_discovery_cases-case328
Unknown
Unknown
Unknown
MRPL13,COL14A1
Controls
Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
engchuan_15_ASD_discovery_controls-control110036018745_
Unknown
RPL35AP19
engchuan_15_ASD_discovery_controls-control110036022051_
Unknown
RPL35AP19
krumm_13_ASD_discovery_controls-control14110.s1
Paternal
Simplex
RN7SKP153,DSCC1,ENPP2,TAF2
nord_11_ASD_discovery_controls-04C27265
0 genes
sanders_11_ASD_discovery_controls-11564.s1
Maternal
Simplex (quad)
NA
COLEC10
sanders_11_ASD_discovery_controls-11794.s1
Both parents
Simplex (quad)
NA
COLEC10
sanders_11_ASD_discovery_controls-11941.s1
Paternal
Simplex (quad)
NA
COLEC10
sanders_11_ASD_discovery_controls-12220.s1
Paternal
Simplex (quad)
NA
sanders_11_ASD_discovery_controls-12261.s1
Paternal
Simplex (quad)
NA
COLEC10
sanders_11_ASD_discovery_controls-12424.s1
Both parents
Simplex (quad)
NA
COLEC10
sanders_11_ASD_discovery_controls-12617.s1
Paternal
Simplex (quad)
NA
sanders_11_ASD_discovery_controls-12617.s1
Paternal
Simplex (quad)
NA
sanders_11_ASD_discovery_controls-13166.s1
Paternal
Simplex (quad)
NA
COLEC10
No Animal Model Data Available


