Variant DetailsVariant: esv2661599Internal ID | 9581018 | Landmark | | Location Information | | Cytoband | 11q13.2 | Allele length | Assembly | Allele length | hg38 | 10181 | hg19 | 10181 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5966184, essv5496368, essv5458623, essv6306018, essv6182676, essv5979798 | Samples | HG00367, HG00232, HG00324, NA11894, HG00269, HG00312 | Known Genes | KDM2A | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | High quality site | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2661599
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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