Detail Information of AutCNV0005113
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: | 6p21.32 | ||||||||||
| Evidences: | CNVs Only Present In Patients; Denovo CNVs; | ||||||||||
| Region: | Chr6: 32509357-32556530 | ||||||||||
| Gain/Loss: | gain | ||||||||||
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 |
|---|---|---|---|
| AutG2290 | FOXG1 | AD | Level 3: The gene has been reported in many families with ASD/autistic features, but the disorder hasn't been a generally acknowledged ASD related disorder. |
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 | ||||
| No data! | |||||||||