Detail Information of AutCNV0000792


Users can click the chromosome coordinates of "Region" label to view information in UCSC Genome Browser.
Ancestry | ADI-R | ADOS | Diagnosis | Family | Individual | Reference | |||||
---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | |||||
Caucasion | ![]() | ![]() | ASD | - | - | - | - | 996 | 1287 | 2283 | Pinto, 2010 |
Population: | - | ||||||||||
Platform: | Illumina Infinium 1M SNP array | ||||||||||
Method: | SNP microarray, qPCR | ||||||||||
Marker: | - | ||||||||||
Band: | 11q22.1 | ||||||||||
Evidences: | |||||||||||
Region: | Chr11: 98907603-98971472 (hg18: Chr11: 98412813-98476682) | ||||||||||
Gain/Loss: | gain |


Abbreviations: AD, autosomal dominant; AR, autosomal recessive; ASD, autism spectrum disorder; ID, intellectual disability; XL, X linked.
Gene ID | Gene Symbol | Inheritance | Evidence Level |
---|---|---|---|
No data! |


Gene ID | Gene Symbol | Evidence Score | Total Score | |||||
---|---|---|---|---|---|---|---|---|
Low-Scale Association | GWAS | Low-Scale Single Gene | Expression | CNV | Linkage | |||
AutG53942 | CNTN5 | 1 | 0 | 0 | 0 | 1 | 1 | 6 |