Variant DetailsVariant: esv3644387Internal ID | 6684454 | Landmark | | Location Information | | Cytoband | 19q13.2 | Allele length | Assembly | Allele length | hg38 | 2838 | hg19 | 2838 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv16056132, essv16056128, essv16056126, essv16056122, essv16056133, essv16056131, essv16056127, essv16056129, essv16056123, essv16056130, essv16056125, essv16056124 | Samples | HG01773, NA20813, NA07048, HG00139, HG01628, HG01519, NA11994, HG01603, NA20828, HG00258, HG01489, HG00259 | Known Genes | | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3644387
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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