Variant DetailsVariant: nsv555187Internal ID | 15995910 | Landmark | | Location Information | | Cytoband | 11q13.1 | Allele length | Assembly | Allele length | hg38 | 74768 | hg19 | 74768 | hg18 | 74768 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv777149 | Samples | | Known Genes | DNAJC4, FERMT3, FKBP2, NUDT22, PLCB3, PPP1R14B, STIP1, TRPT1, VEGFB | 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) | nsv555187
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|