Variant DetailsVariant: essv6071038Internal ID | 9048441 | Landmark | | Location Information | | Cytoband | 7q32.1 | Allele length | Assembly | Allele length | hg38 | 500095 | hg19 | 500095 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | 1 | Merged Status | S | Merged Variants | esv2670312 | Supporting Variants | | Samples | NA19072 | Known Genes | ATP6V1F, CALU, CCDC136, FAM71F1, FAM71F2, FLNC, IRF5, KCP, LINC01000, LOC100130705, METTL2B, OPN1SW, TNPO3 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | essv6071038
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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