Variant DetailsVariant: esv3628325Internal ID | 6668468 | Landmark | | Location Information | | Cytoband | 12p13.33 | Allele length | Assembly | Allele length | hg38 | 4380 | hg19 | 4380 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv14338129, essv14338149, essv14338132, essv14338130, essv14338131, essv14338147, essv14338145, essv14338155, essv14338157, essv14338133, essv14338140, essv14338136, essv14338152, essv14338148, essv14338144, essv14338135, essv14338141, essv14338153, essv14338146, essv14338143, essv14338154, essv14338156, essv14338137, essv14338158, essv14338134, essv14338142, essv14338151, essv14338150, essv14338138, essv14338139 | Samples | HG01060, HG03175, HG02012, HG03452, HG03091, HG02620, HG02549, HG02854, HG03224, NA19917, NA19036, HG02427, HG03394, HG02715, HG02678, NA20126, NA18907, HG02429, NA18912, NA19712, NA19072, HG02721, HG00638, NA19324, HG02580, HG02814, HG03432, NA20348, HG02861, NA19346 | Known Genes | RHNO1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3628325
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 30 | Observed Complex | 0 | Frequency | n/a |
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