Variant DetailsVariant: nssv2763664Internal ID | 17389221 | Landmark | | Location Information | | Cytoband | 17q22 | Allele length | Assembly | Allele length | hg38 | 16319 | hg19 | 16319 | hg18 | 16319 |
| Variant Type | CNV deletion | Copy Number | 1 | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv962452 | Supporting Variants | | Samples | HGDP00456 | Known Genes | TRIM37 | Method | Sequencing | Analysis | Human CNVs | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nssv2763664
| Frequency | Sample Size | 10 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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