Variant DetailsVariant: nsv515629Internal ID | 15096236 | Landmark | | Location Information | | Cytoband | 14q32.2 | Allele length | Assembly | Allele length | hg38 | 4472 | hg19 | 4472 | hg18 | 4472 | hg17 | 4472 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv672617, nssv668421, nssv662318, nssv657771, nssv673601, nssv669173, nssv664161, nssv686867, nssv667265, nssv678093, nssv674250, nssv659713 | Samples | | Known Genes | BDKRB2 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv515629
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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