Variant DetailsVariant: esv3621361Internal ID | 6661540 | Landmark | | Location Information | | Cytoband | 9q31.2 | Allele length | Assembly | Allele length | hg38 | 885 | hg19 | 885 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13593264, essv13593272, essv13593265, essv13593261, essv13593267, essv13593270, essv13593269, essv13593268, essv13593271, essv13593262, essv13593266, essv13593263 | Samples | NA21100, NA20894, HG03873, NA12348, HG01398, HG01092, NA20765, NA21113, NA21123, NA21102, HG03998, HG01786 | Known Genes | TMEM38B | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3621361
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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