Variant DetailsVariant: nsv524492Internal ID | 15105099 | Landmark | | Location Information | | Cytoband | 16q22.1 | Allele length | Assembly | Allele length | hg38 | 120521 | hg19 | 120521 | hg18 | 120521 | hg17 | 120521 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv700430 | Samples | | Known Genes | E2F4, ELMO3, EXOC3L1, FHOD1, KCTD19, KIAA0895L, LRRC29, MIR328, NOL3, PLEKHG4, SLC9A5, TMEM208 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv524492
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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