Variant DetailsVariant: esv3624238 Internal ID | 6664405 | Landmark | | Location Information | | Cytoband | 10q23.33 | Allele length | Assembly | Allele length | hg38 | 1131 | hg19 | 1131 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13899661, essv13899658, essv13899641, essv13899642, essv13899645, essv13899665, essv13899664, essv13899650, essv13899663, essv13899643, essv13899655, essv13899646, essv13899638, essv13899651, essv13899640, essv13899662, essv13899654, essv13899660, essv13899647, essv13899653, essv13899644, essv13899656, essv13899659, essv13899648, essv13899639, essv13899649, essv13899657, essv13899637, essv13899652 | Samples | HG03163, HG01079, HG02433, HG03168, HG02485, HG02645, NA19384, NA20291, HG03520, NA19207, HG03267, NA19451, HG02977, HG03132, NA19462, HG03547, HG01630, HG03123, HG03078, HG03571, NA19099, HG03391, HG01890, HG01107, NA19834, HG02923, HG03157, HG03063, HG03376 | Known Genes | MYOF | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3624238
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 29 | Observed Complex | 0 | Frequency | n/a |
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