Fig. 1From: A crowdsourcing database for the copy-number variation of the Spanish populationCNVs overlapping between SPACNACS and other databases. Comparative between the CNVs found in SPACNACS and the ones present in the 1000 genomes and Gnomad databases. The X axis incrementally represents the level of overlap between the CNVs compared, which range from 0 (CNVs unique to SPACNACS) up to 100% (CNVS with a perfect match)Back to article page