Variant DetailsVariant: esv3612864Internal ID | 6653076 | Landmark | | Location Information | | Cytoband | 7p14.1 | Allele length | Assembly | Allele length | hg38 | 6156 | hg19 | 6156 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv12740675, essv12740674, essv12740676, essv12740681, essv12740680, essv12740678, essv12740682, essv12740677, essv12740679 | Samples | NA19700, HG02012, NA18916, NA19184, NA19391, HG02429, NA18858, HG02722, HG03077 | Known Genes | NME8 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3612864
| Frequency | Sample Size | 2504 | Observed Gain | 9 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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