Detail Information of AutCNV0000672
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 | 1 | 1 | - | - | - | - | - | Vorstman, 2010 |
| Population: | Netherlands | ||||||||||
| Platform: | 550K Illumina SNP array | ||||||||||
| Method: | FISH, SNP microarray | ||||||||||
| Marker: | - | ||||||||||
| Band: | 13q21.2 | ||||||||||
| Evidences: | Overlapping/Recurrent CNVs; | ||||||||||
| Region: | Chr13: 53886995-64184453 (hg18: Chr13: 52784996-63082454) | ||||||||||
| 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