Variant DetailsVariant: esv2661962 Internal ID | 9581381 | Landmark | | Location Information | | Cytoband | 11q24.1 | Allele length | Assembly | Allele length | hg38 | 1051 | hg19 | 1051 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6455496, essv6064282, essv5934596, essv5521366, essv5773591, essv5907307, essv6153398, essv6526606, essv5700844, essv5863626, essv6443921, essv6116483, essv5903778, essv5482645, essv5803813, essv6180483, essv6574921, essv6574621, essv5907897, essv6060977, essv6136100, essv5743278, essv5420016, essv5995678, essv6002476, essv6005612, essv5834978, essv6461939, essv6385646, essv6193765, essv5403166, essv6299003, essv5716769 | Samples | NA18924, NA19204, NA19704, NA18486, NA18504, NA20346, NA19379, NA19916, NA18960, NA18916, NA19313, NA19130, NA18874, NA19317, NA19200, NA19247, NA19707, NA19462, NA19788, NA19449, NA19625, NA19436, NA18974, NA19712, NA19747, NA19444, NA19331, NA19144, NA19334, NA20348, NA19093, NA18488, NA19431 | Known Genes | C11orf63 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | High quality site | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2661962
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 33 | Observed Complex | 0 | Frequency | n/a |
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