Variant DetailsVariant: nsv515847Internal ID | 15096454 | Landmark | | Location Information | | Cytoband | 11p15.3 | Allele length | Assembly | Allele length | hg38 | 3329 | hg19 | 3329 | hg18 | 3329 | hg17 | 3329 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv687787, nssv658142, nssv654912, nssv663639, nssv679637, nssv654604, nssv670981, nssv662310, nssv665005, nssv665113, nssv690012, nssv668660, nssv699259, nssv669088, nssv693824, nssv686440 | Samples | | Known Genes | DKK3 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv515847
| Frequency | Sample Size | 2026 | Observed Gain | 8 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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