Variant DetailsVariant: nssv780547Internal ID | 15727817 | Landmark | | Location Information | | Cytoband | 11q14.3 | Allele length | Assembly | Allele length | hg38 | 118594 | hg19 | 118594 | hg18 | 118594 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv555835 | Supporting Variants | | Samples | | Known Genes | CHORDC1, DISC1FP1 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nssv780547
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|