Variant DetailsVariant: nsv553537Internal ID | 15994260 | Landmark | | Location Information | | Cytoband | 11p15.3 | Allele length | Assembly | Allele length | hg38 | 7701 | hg19 | 7701 | hg18 | 7701 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv768191, nssv768188, nssv768179, nssv768180, nssv768182, nssv768186, nssv768187, nssv768181, nssv768189, nssv768183, nssv768178, nssv768185, nssv768184, nssv768190 | Samples | | Known Genes | USP47 | 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) | nsv553537
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 14 | Observed Complex | 0 | Frequency | n/a |
|
|