Detail Information of AutCNV0004782


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 | |||||
- | ![]() | ![]() | ASD | - | - | - | - | 187 | - | 187 | Bonora E, 2014 |
Population: | - | ||||||||||
Platform: | Agilent 44K | ||||||||||
Method: | array-CGH | ||||||||||
Marker: | - | ||||||||||
Band: | 17q23.2 | ||||||||||
Evidences: | CNVs Only Present In Patients; | ||||||||||
Region: | Chr17: - (hg18: Chr17: 56464-56682) | ||||||||||
Gain/Loss: | loss |


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! |