Variant DetailsVariant: esv3627774 Internal ID | 6667921 | Landmark | | Location Information | | Cytoband | 11q23.2 | Allele length | Assembly | Allele length | hg38 | 2580 | hg19 | 2580 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv14287990, essv14287981, essv14288005, essv14287975, essv14288011, essv14287992, essv14287987, essv14287998, essv14287986, essv14288003, essv14287982, essv14287991, essv14287993, essv14288004, essv14287985, essv14287989, essv14287979, essv14287977, essv14288001, essv14288012, essv14288008, essv14288013, essv14288007, essv14287984, essv14287994, essv14287999, essv14287972, essv14288010, essv14288002, essv14287988, essv14287973, essv14287995, essv14287996, essv14288000, essv14288009, essv14287978, essv14287974, essv14287997, essv14287976, essv14287980, essv14287983, essv14288006 | Samples | HG02890, HG02628, NA20274, HG02589, HG03572, HG02811, NA19764, NA18923, HG02840, NA19916, HG02860, NA20287, NA19137, HG02642, HG02571, HG02882, HG03048, NA19707, HG02678, HG02449, HG02887, NA20126, HG03136, HG03078, NA18856, HG02881, NA19318, HG02594, NA19625, NA18858, HG01896, HG02557, NA18517, HG03437, HG02721, HG03565, NA19116, NA19900, HG02861, NA19146, HG02805, HG02808 | Known Genes | NCAM1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3627774
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 42 | Observed Complex | 0 | Frequency | n/a |
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