Variant DetailsVariant: esv3585031Internal ID | 6625349 | Landmark | | Location Information | | Cytoband | 1p36.32 | Allele length | Assembly | Allele length | hg38 | 35185 | hg19 | 35203 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv9841891, essv9841896, essv9841892, essv9841895, essv9841898, essv9841894, essv9841897, essv9841890, essv9841899, essv9841893 | Samples | HG01063, HG03224, HG02315, HG03363, NA19042, HG02256, NA19834, HG02308, NA20348, HG03303 | Known Genes | TTC34 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3585031
| Frequency | Sample Size | 2504 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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