Detail Information of AutCNV0004081


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 | - | - | ASD | 915 | 915 | - | - | - | - | - | Levy, 2011 |
Population: | Simons Simplex Collection | ||||||||||
Platform: | Agilent 244K oligonucleotide CGH microarray, 33K and 38K BAC arrays | ||||||||||
Method: | aCGH | ||||||||||
Marker: | - | ||||||||||
Band: | 7p22.1 | ||||||||||
Evidences: | CNVs Only Present In Patients; | ||||||||||
Region: | Chr7: 6982627-7230016 (hg18: Chr7: 6949152-7196541) | ||||||||||
Gain/Loss: | gain |


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 | |||
AutG56913 | C1GALT1 | 0 | 0 | 0 | 2 | 1 | 0 | 4 |