Variant DetailsVariant: esv2670623 Internal ID | 9590042 | Landmark | | Location Information | | Cytoband | 1q42.3 | Allele length | Assembly | Allele length | hg38 | 185 | hg19 | 185 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6321453, essv6246043, essv6140632, essv6498609, essv6513219, essv6227012, essv5954079, essv5706960, essv6308546, essv6362764, essv5657540, essv6000194, essv5465639, essv6588542, essv6571768, essv6212350, essv6106053, essv5489848, essv6203582, essv5648938, essv5849969, essv5664356, essv5873831, essv5715183, essv5454526, essv6116899, essv6105326, essv6306458, essv5561062, essv6081245, essv5667375, essv6337331, essv5778811, essv5909989, essv6569538, essv6344463, essv5896853, essv6191561, essv5835726, essv5564905, essv6560718 | Samples | HG01441, HG01098, NA19399, HG00318, NA19355, NA19819, NA19393, NA18530, NA20507, HG00337, NA19381, NA18519, HG01366, HG01070, HG00330, NA18547, NA19197, HG01354, NA19771, NA19138, HG00158, NA12761, NA19371, NA19385, HG01048, HG00108, HG00282, HG00344, HG01101, HG00276, NA19395, HG01107, HG00136, HG00278, HG01357, NA19428, HG00259, HG00310, NA19116, HG01378, HG00345 | Known Genes | RBM34 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2670623
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 41 | Observed Complex | 0 | Frequency | n/a |
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