Variant DetailsVariant: esv3620562 Internal ID | 6660743 | Landmark | | Location Information | | Cytoband | 9q21.11 | Allele length | Assembly | Allele length | hg38 | 29809 | hg19 | 29809 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13511489, essv13511487, essv13511482, essv13511491, essv13511477, essv13511476, essv13511471, essv13511478, essv13511484, essv13511486, essv13511490, essv13511474, essv13511475, essv13511480, essv13511473, essv13511472, essv13511483, essv13511479, essv13511492, essv13511488, essv13511485, essv13511481 | Samples | HG00608, HG01438, NA12155, HG03673, NA19457, HG03583, HG00313, HG00268, NA18910, HG00692, HG00324, NA19461, NA19318, NA18952, NA21144, HG02049, NA19835, HG02019, HG02051, HG02805, HG01578, NA19676 | Known Genes | APBA1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3620562
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 22 | Observed Complex | 0 | Frequency | n/a |
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