Variant DetailsVariant: esv3630531 Internal ID | 6670667 | Landmark | | Location Information | | Cytoband | 12q23.1 | Allele length | Assembly | Allele length | hg38 | 15180 | hg19 | 15180 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv14587009, essv14587016, essv14586992, essv14586999, essv14587000, essv14587010, essv14587007, essv14587002, essv14587012, essv14587013, essv14587015, essv14586993, essv14586997, essv14587004, essv14587005, essv14587006, essv14587011, essv14586998, essv14587014, essv14586991, essv14587008, essv14587003, essv14587001, essv14586995, essv14586996, essv14586994, essv14586990 | Samples | HG00157, HG01440, NA20522, HG02006, NA20905, HG00148, NA18546, NA21120, HG01468, NA21106, NA20854, NA20849, HG03672, HG01785, HG03583, HG01668, HG01497, HG01486, HG01356, NA20814, HG01257, HG03702, HG04035, HG03905, NA20872, NA19315, HG04195 | Known Genes | ANKS1B | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3630531
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 27 | Observed Complex | 0 | Frequency | n/a |
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