Variant DetailsVariant: nsv553539 Internal ID | 15994262 | Landmark | | Location Information | | Cytoband | 11p15.3 | Allele length | Assembly | Allele length | hg38 | 503 | hg19 | 503 | hg18 | 503 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv768220, nssv768208, nssv768194, nssv768202, nssv768200, nssv768205, nssv768232, nssv768233, nssv768195, nssv768236, nssv768222, nssv768240, nssv768212, nssv768213, nssv768218, nssv768237, nssv768204, nssv768206, nssv768196, nssv768201, nssv768209, nssv768207, nssv768219, nssv768193, nssv768217, nssv768227, nssv768210, nssv768234, nssv768225, nssv768214, nssv768215, nssv768211, nssv768231, nssv768197, nssv768238, nssv768199, nssv768241, nssv768235, nssv768230, nssv768221, nssv768223, nssv768226, nssv768229, nssv768203, nssv768228, nssv768198, nssv768239, nssv768216, nssv768224 | 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) | nsv553539
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 49 | Observed Complex | 0 | Frequency | n/a |
|
|