Variant DetailsVariant: nsv569924Internal ID | 16010647 | Landmark | | Location Information | | Cytoband | 15q23 | Allele length | Assembly | Allele length | hg38 | 357 | hg19 | 357 | hg18 | 357 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv844975, nssv844973, nssv844982, nssv844981, nssv844976, nssv844980, nssv844989, nssv844987, nssv844988, nssv844978, nssv844972, nssv844974, nssv844985, nssv844990, nssv844983, nssv844977, nssv844986, nssv844971, nssv844984, nssv844979, nssv844970 | Samples | | Known Genes | MYO9A | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nsv569924
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 21 | Observed Complex | 0 | Frequency | n/a |
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