Variant DetailsVariant: nsv517407Internal ID | 15098014 | Landmark | | Location Information | | Cytoband | 11q25 | Allele length | Assembly | Allele length | hg38 | 893 | hg19 | 893 | hg18 | 893 | hg17 | 893 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv664724, nssv653849, nssv670038, nssv664972, nssv668841, nssv666548, nssv662808, nssv657981, nssv653919, nssv673599, nssv664940, nssv652593, nssv658635, nssv653993, nssv663354, nssv663333, nssv693894, nssv667558, nssv654436, nssv658708, nssv654719, nssv684562, nssv665532, nssv691099, nssv657152, nssv654798, nssv652616, nssv685864, nssv665986, nssv653206, nssv684239, nssv663879, nssv667912, nssv678924, nssv677356, nssv656562, nssv658008, nssv660772, nssv661870, nssv693091, nssv685836 | Samples | | Known Genes | OPCML | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517407
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 41 | Observed Complex | 0 | Frequency | n/a |
|
|