Variant DetailsVariant: nsv516064Internal ID | 15096671 | Landmark | | Location Information | | Cytoband | 16q22.1 | Allele length | Assembly | Allele length | hg38 | 51513 | hg19 | 51513 | hg18 | 51513 | hg17 | 51513 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv660991, nssv673651, nssv665949, nssv683506 | Samples | | Known Genes | CBFB | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv516064
| Frequency | Sample Size | 2026 | Observed Gain | 4 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|