Detail Information of AutCNV0000001
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 | 165 | 118 | 47 | 99 | 195 | 196 | 391 | Sebat, 2007 | ||
Population: | USA | ||||||||||
Platform: | Agilent 244K array, 390K ROMA array | ||||||||||
Method: | aCGH | ||||||||||
Marker: | - | ||||||||||
Band: | 2q24.2 | ||||||||||
Evidences: | Denovo CNVs; | ||||||||||
Region: | Chr2: 162387213-162486465 (hg17: Chr2: 162212720-162311972) | ||||||||||
Gain/Loss: | loss |
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
Gene ID | Gene Symbol | Evidence Score | Total Score | ||||||
---|---|---|---|---|---|---|---|---|---|
Low-Scale Association | GWAS | Low-Scale Single Gene | Expression | CNV | Linkage | ||||
No data! |