Variant DetailsVariant: nsv518289Internal ID | 15098896 | Landmark | | Location Information | | Cytoband | 15q25.2 | Allele length | Assembly | Allele length | hg38 | 406562 | hg19 | 281041 | hg18 | 291041 | hg17 | 291041 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv695720 | Samples | | Known Genes | DNM1P41, GOLGA6L4, GOLGA6L5P, LINC00933, LOC100505679, LOC388152, LOC440300, LOC642423, UBE2Q2P1 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv518289
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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