Variant DetailsVariant: esv3620382Internal ID | 6660565 | Landmark | | Location Information | | Cytoband | 9p13.3 | Allele length | Assembly | Allele length | hg38 | 1607 | hg19 | 1607 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13459411, essv13459412, essv13459414, essv13459410, essv13459409, essv13459415, essv13459416, essv13459413 | Samples | NA19648, HG02727, HG03926, NA12058, HG02792, HG02789, HG00155, NA12830 | Known Genes | ARHGEF39 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3620382
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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