Detail Information of AutCNV0005692
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 | |||||
| Canadian |  | | ASD | 200 | - | - | - | 200 | - | - | Yuen RK, 2016 |
| Population: | - | ||||||||||
| Platform: | Hiseq2000 | ||||||||||
| Method: | WGS | ||||||||||
| Marker: | - | ||||||||||
| Band: | |||||||||||
| Evidences: | CNVs Only Present In Patients; Denovo CNVs; | ||||||||||
| Region: | Chr2: - | ||||||||||
| Gain/Loss: | Loss | ||||||||||
2. Related Syndromic Genes TopAbbreviations: 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| Gene ID | Gene Symbol | Evidence Score | Total Score | |||||
|---|---|---|---|---|---|---|---|---|
| Low-Scale Association | GWAS | Low-Scale Single Gene | Expression | CNV | Linkage | |||
| AutG54221 | SNTG2 | 0 | 0 | 1 | 0 | 1 | 1 | 14 |