Variant DetailsVariant: esv3623921Internal ID | 6664088 | Landmark | | Location Information | | Cytoband | 10q22.3 | Allele length | Assembly | Allele length | hg38 | 107587 | hg19 | 107587 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13868341, essv13868345, essv13868343, essv13868338, essv13868337, essv13868342, essv13868344, essv13868340, essv13868339 | Samples | HG02275, NA19795, HG02277, HG02017, HG02271, NA11994, HG01892, NA19654, HG02006 | Known Genes | BEND3P3, NUTM2B | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3623921
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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