Detail Information of AutCNV0003329
1. Sample AND Method Top
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 | - | - | autism | - | - | - | - | 1224 | 3801 | 5025 | Gai, 2011 |
Population: | AGRE | ||||||||||
Platform: | Illumina Infinium II Human-Hap550 array | ||||||||||
Method: | SNP microarray | ||||||||||
Marker: | - | ||||||||||
Band: | 11q13.2 | ||||||||||
Evidences: | CNVs Only Present In Patients; | ||||||||||
Region: | Chr11: 67352689-67715028 | ||||||||||
Gain/Loss: | gain |
2. Related Syndromic Genes Top
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! |
3. Related Non-syndromic Genes Top