Variant DetailsVariant: esv2661194Internal ID | 9580613 | Landmark | | Location Information | | Cytoband | 10p12.1 | Allele length | Assembly | Allele length | hg38 | 8289 | hg19 | 8289 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6401067, essv5396510, essv5595042, essv5902449, essv5764771, essv6172249, essv5779340, essv5807224 | Samples | NA19332, NA19446, HG00641, NA18489, NA19457, NA19908, NA19437, NA19093 | Known Genes | MPP7 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | High quality site | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2661194
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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