I am currently working with four independent datasets with imputation genotypes, and I was trying to merge the SNPs into a single genotypic matrix. However I found a individual was missing after using PLINK 1.9 merge-list command without any relevant information given. Any suggestions for this situation?
Here is the log.
(C) 2005-2019 Shaun Purcell, Christopher Chang GNU General Public License v3
Logging to MergeNoFlip.log.
Options in effect:
--merge-list MergeNoflip.list
--out MergeNoFlip
773821 MB RAM detected; reserving 386910 MB for main workspace.
Allocated 122420 MB successfully, after larger attempt(s) failed.
Warning: Variants '1:62777:A:T' and '1:62777' have the same position.
Warning: Variants '1:95440:C:G' and '1:95440' have the same position.
Warning: Variants '1:173052:C:A' and '1:173052' have the same position.
35128 more same-position warnings: see log file.
Performing single-pass merge (6380 people, 6261375 variants).
Merged fileset written to MergeNoFlip.bed + MergeNoFlip.bim + MergeNoFlip.fam .
The four datasets included in merge list contain totally 6,381 samples. But only 6,380 samples left after merging.
Appreciate any help.