Detail Information of AutCNV0005118
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 | |||||
- | autism | 83 | - | - | - | 257 | 288 | 545 | Kanduri C, 2016 | ||
Complication: | Y | ||||||||||
Population: | Finnish | ||||||||||
Platform: | Illumina Human OmniExpress-12v1.0 beadchip (730K) | ||||||||||
Method: | - | ||||||||||
Marker: | - | ||||||||||
Band: | 16p13.3 | ||||||||||
Evidences: | CNVs Only Present In Patients; | ||||||||||
Region: | Chr16: 7757373-7776124 | ||||||||||
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