Variant DetailsVariant: nsv516003Internal ID | 15096610 | Landmark | | Location Information | | Cytoband | 12p13.33 | Allele length | Assembly | Allele length | hg38 | 5025 | hg19 | 5025 | hg18 | 5025 | hg17 | 5025 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv665662, nssv682484, nssv693566, nssv671144, nssv681116, nssv678091, nssv698086 | Samples | | Known Genes | | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv516003
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
|
|