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High-resolution Copy Number Variation (CNV) Discovery - CNVE calls
The regions made available in this provisional data release are the chromosomal start and end coordinates of 8,599 copy number variation events (CNVEs), which are representative of the underlying sample level CNV calls. Briefly, clusters of overlapping CNVs at the sample level are merged into CNVE if they have at least 51% of reciprocal overlap. This means that CNV calls with similar boundaries are merged, while overlapping CNVs of very different size or different start and end points will be kept separated also at the CNVE level. Overlapping CNVEs will therefore be present in the dataset. Each of the CNVEs in this provisional data release has some level of independent validation, either by an independent platform or by overlap with other published datasets.
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