Detail Information of AutCNV0004822
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 | - | - | - | - | 49 | - | 49 | Mizuno M, 2015 | ||
Complication: | Y | ||||||||||
Population: | Japanese | ||||||||||
Platform: | Agilent Human genome CGH 180K | ||||||||||
Method: | aCGH | ||||||||||
Marker: | - | ||||||||||
Band: | 19q13.33 | ||||||||||
Evidences: | CNVs Only Present In Patients; Denovo CNVs; | ||||||||||
Region: | Chr19: - | ||||||||||
Gain/Loss: | gain |
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 | |||
AutG4909 | NTF4 | 1 | 0 | 0 | 0 | 1 | 1 | 6 |