Variant DetailsVariant: esv2724584 Internal ID | 9958886 | Landmark | | Location Information | | Cytoband | 1q42.13 | Allele length | Assembly | Allele length | hg38 | 463 | hg19 | 463 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6902717, essv6704015, essv6950743, essv6892485, essv6789348, essv6781067, essv6710755, essv6786253, essv6968130, essv6889174, essv6821361, essv6692973, essv6804562, essv6898764, essv6726027, essv6955036, essv6961838, essv6718334, essv6871863 | Samples | SSM100, SSM027, SSM046, SSM079, SSM097, SSM013, SSM009, SSM074, SSM042, SSM028, SSM026, SSM044, SSM068, SSM040, SSM037, SSM091, SSM070, SSM025, SSM098 | Known Genes | GALNT2 | 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) | esv2724584
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 19 | Observed Complex | 0 | Frequency | n/a |
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