Detail Information of AutCNV0004899
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 | |||||
- | - | - | ASD | - | - | - | - | 3724 | - | 3724 | Hu J, 2015 |
Complication: | Y | ||||||||||
Population: | - | ||||||||||
Platform: | NimbleGen 135K oligonucleotide array; SignatureChip Oligo Solution version 2.0 | ||||||||||
Method: | aCGH;FISH | ||||||||||
Marker: | - | ||||||||||
Band: | 3p26.3 | ||||||||||
Evidences: | CNVs Only Present In Patients; | ||||||||||
Region: | Chr3: - (hg18: Chr3: 1322292-1447530) | ||||||||||
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