Variant DetailsVariant: esv2673027Internal ID | 9592446 | Landmark | | Location Information | | Cytoband | 7p15.3 | Allele length | Assembly | Allele length | hg38 | 752855 | hg19 | 752855 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5918897 | Samples | NA18986 | Known Genes | FAM221A, NPY, STK31 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2673027
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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