Detail Information of AutCNV0000561


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 | - | - | - | - | 119 | 54 | 173 | Gregory, 2009 |
Population: | USA | ||||||||||
Platform: | Genetix Qarray2 | ||||||||||
Method: | aCGH | ||||||||||
Marker: | - | ||||||||||
Band: | 11p15.5 | ||||||||||
Evidences: | Overlapping/Recurrent CNVs; | ||||||||||
Region: | Chr11: 60001-828406 | ||||||||||
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 |
---|---|---|---|
AutG3265 | HRAS | AD | Level 1: The gene has only been reported in single cases with ASD/autistic features. Additional evidences are needed. |

