Variant DetailsVariant: esv2669590Internal ID | 9589009 | Landmark | | Location Information | | Cytoband | Xp22.2 | Allele length | Assembly | Allele length | hg38 | 203 | hg19 | 203 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6100817, essv5710389, essv5659894, essv5923906 | Samples | HG00654, NA18571, NA18557, NA18637 | Known Genes | PIR, PIR-FIGF | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2669590
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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