Currently instead of downloading the genotypes of one study, all the available genotypes for an inversion from all the different studies are merged into a single file (including for example those experimentally validated and imputed from tag SNPs for HsInv0379).
Currently instead of downloading the genotypes of one study, all the available genotypes for an inversion from all the different studies are merged into a single file (including for example those experimentally validated and imputed from tag SNPs for HsInv0379).