Variant DetailsVariant: nsv587694 Internal ID | 16028417 | Landmark | | Location Information | | Cytoband | 21q22.3 | Allele length | Assembly | Allele length | hg38 | 2637 | hg19 | 2637 | hg18 | 2637 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv947910, nssv947948, nssv947957, nssv947950, nssv947909, nssv947959, nssv947943, nssv947952, nssv947962, nssv947944, nssv947946, nssv947941, nssv947937, nssv947930, nssv947953, nssv947925, nssv947942, nssv947947, nssv947951, nssv947938, nssv947931, nssv947921, nssv947913, nssv947932, nssv947945, nssv947918, nssv947911, nssv947908, nssv947912, nssv947960, nssv947928, nssv947924, nssv947933, nssv947916, nssv947958, nssv947935, nssv947914, nssv947927, nssv947915, nssv947934, nssv947926, nssv947956, nssv947906, nssv947907, nssv947922, nssv947964, nssv947920, nssv947917, nssv947963, nssv947919, nssv947929, nssv947923, nssv947905, nssv947961, nssv947954, nssv947955, nssv947949, nssv947936, nssv947939, nssv947940 | Samples | | Known Genes | HSF2BP | 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) | nsv587694
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 60 | Observed Complex | 0 | Frequency | n/a |
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