Detail Information of AutCNV0000303


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 | - | - | - | - | 1 | - | 1 | Gilling, 2008 |
Complication: | high-grade myopia | ||||||||||
Population: | Denmark | ||||||||||
Platform: | - | ||||||||||
Method: | aCGH | ||||||||||
Marker: | - | ||||||||||
Band: | 18q12 | ||||||||||
Evidences: | Denovo CNVs; | ||||||||||
Region: | Chr18: 31943002-35138002 (hg17: Chr18: 30197000-33392000) | ||||||||||
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! |

