Detail Information of AutCNV0000197


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 | ![]() | ![]() | ASD | - | - | - | - | 1 | - | 1 | Daniel, 2007 |
Population: | - | ||||||||||
Platform: | BlueGnome Cytochip 4102 array | ||||||||||
Method: | SNP microarray | ||||||||||
Marker: | - | ||||||||||
Band: | 13q21.1-21.32 | ||||||||||
Evidences: | CNVs Only Present In Patients; | ||||||||||
Region: | Chr13: 58692746-69244173 (hg15: Chr13: 57629383-68180810) | ||||||||||
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! |

