Detail Information of AutCNV0005092


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 | |||||
Chinese | ![]() | ![]() | ASD | - | - | - | - | 68 | - | 68 | Siu WK, 2016 |
Complication: | Y | ||||||||||
Population: | Hong?Kong | ||||||||||
Platform: | NimbleGen CGX-135K oligonucleotide array | ||||||||||
Method: | array?CGH | ||||||||||
Marker: | - | ||||||||||
Band: | 6q14.1 | ||||||||||
Evidences: | CNVs Only Present In Patients; | ||||||||||
Region: | Chr6: 82844151-83486991 | ||||||||||
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 | ||||
No data! |