Variant DetailsVariant: esv3627773Internal ID | 6667920 | Landmark | | Location Information | | Cytoband | 11q23.2 | Allele length | Assembly | Allele length | hg38 | 11655 | hg19 | 11655 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv14287967, essv14287969, essv14287966, essv14287971, essv14287970, essv14287968 | Samples | HG01412, HG01348, HG01455, HG01200, HG01113, HG01111 | Known Genes | NCAM1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3627773
| Frequency | Sample Size | 2504 | Observed Gain | 6 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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