Variant DetailsVariant: nsv971192Internal ID | 18259726 | Landmark | | Location Information | | Cytoband | 7p15.3 | Allele length | Assembly | Allele length | hg38 | 2237 | hg19 | 2237 | hg18 | 2237 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2759607 | Samples | HGDP00456 | Known Genes | ITGB8 | Method | Sequencing | Analysis | Human CNVs | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv971192
| Frequency | Sample Size | 10 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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