Variant DetailsVariant: nsv515825Internal ID | 15096432 | Landmark | | Location Information | | Cytoband | 16q23.3 | Allele length | Assembly | Allele length | hg38 | 6130 | hg19 | 6130 | hg18 | 6130 | hg17 | 6130 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv689454, nssv683319, nssv672862, nssv680615, nssv684616, nssv664894, nssv688293, nssv671890, nssv682019, nssv665647, nssv674120, nssv665331, nssv685639, nssv663421 | Samples | | Known Genes | CDH13 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv515825
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 14 | Observed Complex | 0 | Frequency | n/a |
|
|