Detail Information of AutCNV0000265


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 | |||||
Not Mentioned | ![]() | ![]() | autism | - | - | - | - | 1 | - | 1 | Smith, 2002 |
Complication: | auditory processing deficits | ||||||||||
Population: | - | ||||||||||
Platform: | - | ||||||||||
Method: | FISH | ||||||||||
Marker: | - | ||||||||||
Band: | 13q12-13 | ||||||||||
Evidences: | CNVs Only Present In Patients; | ||||||||||
Region: | Chr13: 29623000-39160000 | ||||||||||
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! |

