Variant DetailsVariant: esv3626707Internal ID | 6666855 | Landmark | | Location Information | | Cytoband | 11q13.2 | Allele length | Assembly | Allele length | hg38 | 10018 | hg19 | 10018 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv14197400, essv14197397, essv14197396, essv14197399, essv14197398, essv14197401 | Samples | HG00367, HG00232, HG01684, HG00324, NA11894, HG00269 | Known Genes | KDM2A | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3626707
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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