Detail Information of AutCNV0005101


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 | |||||
- | ![]() | ![]() | autistic | - | - | - | - | 1 | - | 1 | Balay L, 2016 |
Complication: | Y | ||||||||||
Population: | - | ||||||||||
Platform: | Affymetrix Genome-Wide Human CytoScan HD SNP Array | ||||||||||
Method: | SNP Array | ||||||||||
Marker: | - | ||||||||||
Band: | 11p13 | ||||||||||
Evidences: | CNVs Only Present In Patients; | ||||||||||
Region: | Chr11: 31452082-31615319 | ||||||||||
Gain/Loss: | loss |


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! |


Gene ID | Gene Symbol | Evidence Score | Total Score | ||||||
---|---|---|---|---|---|---|---|---|---|
Low-Scale Association | GWAS | Low-Scale Single Gene | Expression | CNV | Linkage | ||||
No data! |