Detail Information of AutCNV0005117


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 | |||||
- | ![]() | ![]() | autism | 83 | - | - | - | 257 | 288 | 545 | Kanduri C, 2016 |
Complication: | Y | ||||||||||
Population: | Finnish | ||||||||||
Platform: | Illumina Human OmniExpress-12v1.0 beadchip (730K) | ||||||||||
Method: | - | ||||||||||
Marker: | - | ||||||||||
Band: | 15q13.2q13.3 | ||||||||||
Evidences: | CNVs Only Present In Patients; | ||||||||||
Region: | Chr15: 30936285-32514341 | ||||||||||
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 | |||
AutG54715 | RBFOX1 | 0 | 0 | 2 | 2 | 1 | 2 | 28 |