Variant DetailsVariant: nsv584755Internal ID | 16025478 | Landmark | | Location Information | | Cytoband | 2q37.3 | Allele length | Assembly | Allele length | hg38 | 58898 | hg19 | 58898 | hg18 | 58898 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv7348n54 | Supporting Variants | nssv1152351 | Samples | HGDP00546 | Known Genes | ESPNL, ILKAP, KLHL30 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nsv584755
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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