Variant DetailsVariant: esv2726828 Internal ID | 9961136 | Landmark | | Location Information | | Cytoband | 4p16.3 | Allele length | Assembly | Allele length | hg38 | 527 | hg19 | 527 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6962717, essv6951321, essv6774110, essv6926302, essv6825761, essv6836860, essv6789895, essv6794059, essv6955988, essv6850165, essv6689901, essv6821863, essv6785784, essv6892953, essv6840678, essv6726546, essv6770251, essv6813800, essv6722697, essv6973705, essv6781629, essv6718826, essv6942656, essv6886514, essv6730316, essv6683436, essv6833242, essv6700417, essv6798233, essv6707891, essv6679868, essv6693567 | Samples | SSM036, SSM083, SSM071, SSM027, SSM045, SSM046, SSM011, SSM079, SSM065, SSM039, SSM041, SSM023, SSM084, SSM047, SSM069, SSM029, SSM096, SSM026, SSM019, SSM044, SSM033, SSM066, SSM068, SSM072, SSM082, SSM080, SSM037, SSM077, SSM070, SSM025, SSM034, SSM098 | Known Genes | FAM53A | Method | Sequencing | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | Platform | Illumina HiSeq 2000 | Comments | | Reference | Wong_et_al_2012b | Pubmed ID | 23290073 | Accession Number(s) | esv2726828
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 32 | Observed Complex | 0 | Frequency | n/a |
|
|