Variant DetailsVariant: esv3633556Internal ID | 6673678 | Landmark | | Location Information | | Cytoband | 13q34 | Allele length | Assembly | Allele length | hg38 | 141986 | hg19 | 141986 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv373e214 | Supporting Variants | essv14898500, essv14898501, essv14898498, essv14898499, essv14898502 | Samples | NA11829, HG00145, HG04054, HG03846, HG03060 | Known Genes | ARHGEF7 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3633556
| Frequency | Sample Size | 2504 | Observed Gain | 5 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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