Variant DetailsVariant: esv3622394Internal ID | 6662564 | Landmark | | Location Information | | Cytoband | 10p13 | Allele length | Assembly | Allele length | hg38 | 8089 | hg19 | 8089 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13697861, essv13697860, essv13697863, essv13697862, essv13697864 | Samples | HG00138, HG02490, HG02736, HG00708, NA07056 | Known Genes | CCDC3 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3622394
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
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