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Genome-wide representation of the common structural variants in the FTD/ALS case-control cohort
Manhattan plot depicting the GWAS results (n = 2,307 FTD and 3,677 controls, and 4,699 structural variants with MAF ≥ 1%). The annotations show the break-end variant on chromosome 9, corresponding to the C9orf72 hexanucleotide repeat expansion, and a 673-kb complex inversion that is part of the MAPT H2 haplotype.
