Variant DetailsVariant: nsv965411Internal ID | 18253959 | Landmark | | Location Information | | Cytoband | 3q28 | Allele length | Assembly | Allele length | hg38 | 7497 | hg19 | 7497 | hg18 | 7497 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2762602, nssv2765626, nssv2758948 | Samples | HGDP00998, HGDP00521, HGDP00927 | Known Genes | CCDC50 | Method | Sequencing | Analysis | Human CNVs | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv965411
| Frequency | Sample Size | 10 | Observed Gain | 0 | Observed Loss | 3 | Observed Complex | 0 | Frequency | n/a |
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