sqnm-client.pl result for Sequenom genotype file:
 test.xls

MARKER  	#Call	#Fail	Total	%_OK	Chr	hg18_position	NCBI_info
rs10116	721	15	736	97.96	chr2	65350233	ACTR2 LOC10097 mrna-utr 
rs10115	721	15	736	97.96	chr3	133559819	ACPP LOC55 mrna-utr 
rs10117	716	20	736	97.28	chr5	137920069	HSPA9 LOC3313 reference coding-synonymous 
rs10110	722	14	736	98.10	chr9	139569403	WDR85 LOC92715 mrna-utr 
rs10111	659	77	736	89.54	chr11	118391327	RPS25 LOC6230 locus-region CCDC84 LOC338657 reference coding-synonymous 
rs10114	722	14	736	98.10	chr17	3652520	ITGAE LOC3682 intron 
rs10112	712	24	736	96.74	chr17	7706249	CYB5D1 LOC124637 mrna-utr 
rs10113	717	19	736	97.42	chr19	51804488	CALM3 LOC808 mrna-utr 

Overall success for 8 markers: 96.64% 
	(5690 calls, 198 failures, 5888 attempts)

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There were 15 duplicate samples detected. 
A summary of the duplicate analyses was written to file:
	test.xls_DUPL.txt

File test.xls_gt.txt lists markers across the top,
sample names in first column, and their genotypes in all others. 
Missing genotypes are blank.


Each marker.txt file has six columns, tab-delimited:

	PLATE    =      local name for the multiplex/chip  

	WELL_POSITION   = 384-well format

	ASSAY_ID        = SNP name

	GENOTYPE_ID     = call (different formats available)
		 homozygotes are listed as a single base or
		 with two bases separated by a space, comma, or slash.

	DESCRIPTION     = call description that includes an
		 indication of confidence,
		 where 'Conservative' and 'Moderate' are 
		 considered very good, 'aggressive' OK, 
		 and rest are not accepted for report, 
		 unless manually called.

	SAMPLE_ID       = your submitted sample ID

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