Variant DetailsVariant: nsv569928 Internal ID | 16010651 | Landmark | | Location Information | | Cytoband | 15q23 | Allele length | Assembly | Allele length | hg38 | 1719 | hg19 | 1719 | hg18 | 1719 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv845004, nssv845036, nssv845018, nssv845021, nssv845031, nssv845040, nssv845037, nssv845044, nssv845039, nssv845027, nssv845045, nssv845022, nssv845033, nssv845009, nssv845013, nssv845005, nssv845016, nssv845029, nssv845042, nssv845014, nssv845003, nssv845043, nssv845038, nssv845041, nssv845008, nssv845007, nssv845015, nssv845032, nssv845028, nssv845012, nssv845025, nssv845017, nssv845034, nssv845010, nssv845026, nssv845035, nssv845023, nssv845030, nssv845046, nssv845011, nssv845006, nssv845019, nssv845024, nssv845020 | 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) | nsv569928
| Frequency | Sample Size | 17421 | Observed Gain | 31 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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