Variant DetailsVariant: esv2675710Internal ID | 9595129 | Landmark | | Location Information | | Cytoband | 3p12.3 | Allele length | Assembly | Allele length | hg38 | 929 | hg19 | 929 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6062824, essv6050737, essv6272133, essv5747965, essv6515449, essv5398974, essv6327680, essv6200017, essv6089253, essv6530651, essv5957441, essv6320790, essv6003523, essv5997827, essv6055024 | Samples | HG00361, HG01359, HG01374, HG00566, HG00702, HG01365, HG01069, HG01080, HG00534, NA18856, NA19452, HG01075, NA19440, HG01375, HG01055 | Known Genes | ROBO2 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2675710
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 15 | Observed Complex | 0 | Frequency | n/a |
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