Variant DetailsVariant: esv2722965Internal ID | 9957265 | Landmark | | Location Information | | Cytoband | 20q13.33 | Allele length | Assembly | Allele length | hg38 | 877 | hg19 | 877 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6777376, essv6713861, essv6921236, essv6913599, essv6835784, essv6967344, essv6729236, essv6804183, essv6784580, essv6816245, essv6895490, essv6807080, essv6741841, essv6846649, essv6780576, essv6758834, essv6692392, essv6756255, essv6769217, essv6863512, essv6696593, essv6882999, essv6914263, essv6941370, essv6716532, essv6744659, essv6693576, essv6937210, essv6717766, essv6885707, essv6841198, essv6813654, essv6824574, essv6773062, essv6871405, essv6666325, essv6733102, essv6902175, essv6674677, essv6954283, essv6946852, essv6710294, essv6780423, essv6750336, essv6877378, essv6905779, essv6832211, essv6699366, essv6898308, essv6960892, essv6810082, essv6917026, essv6880158, essv6788759, essv6706967, essv6950098, essv6678780 | Samples | SSM059, SSM036, SSM008, SSM027, SSM024, SSM075, SSM046, SSM064, SSM079, SSM065, SSM038, SSM013, SSM009, SSM073, SSM093, SSM074, SSM042, SSM088, SSM002, SSM041, SSM058, SSM092, SSM090, SSM021, SSM047, SSM069, SSM029, SSM026, SSM017, SSM094, SSM032, SSM003, SSM031, SSM067, SSM001, SSM006, SSM085, SSM068, SSM081, SSM040, SSM082, SSM015, SSM016, SSM053, SSM005, SSM037, SSM077, SSM022, SSM010, SSM095, SSM025, SSM099, SSM043, SSM052, SSM098, SSM056, SSM012 | Known Genes | ZGPAT | 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) | esv2722965
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 57 | Observed Complex | 0 | Frequency | n/a |
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