Table 1. Basic characteristics of the selected microsatellite markers.

Panel	Marker	Chr: position	Repeat unit	Labeled primer sequence (5′-3′)	Unlabeled primer sequence (5′-3′)*	Conc. (μM)	No. alleles (range)
CNA2	CNA2A	11: 389201–389350	CT	FAM- CGAGGTCATGTTGTGAGTCC	G TGACCGTCTCGTTCTTCTCA	0.3	15 (10–60)
	CNA2B	9: 191563–191711	TG	HEX- TCGTCAACGATGCAAGTCTC	GGGCCTGGGAAATAGGTAGA	0.3	6 (8–21)
	CNA2C	10: 307773–306912	TA	TET- AGAAGCACATGGGGAAAGG	GCGCAGTTTGAAGATGAGAA	1.0	16 (8–44)
CNA3	CNA3A	11: 1281429–12814716	CTA	FAM- ACCCCCTGCCCATCATA	GCACAGGCATAAAGCTAAGTGTGA	0.3	9 (19–69)
	CNA3B	4: 339525–339664	TCT	HEX- TGGGGATATCGATTCCTTCTC	GATTGGTATGGGAAGCGTTG	0.3	5 (5–17)
	CNA3C	7: 285123–285270	CCA	TET- TGGAAGAGGATGGAGCGTAT	GCATAGTTTATCGTTTTCTCTTTTC	0.3	10 (8–38)
CNA4	CNA4A	5: 233120–233445	TTAT	FAM- CGTCGAAGACTGCACAAAAA	GTTCTGTATGACAGGTCGCAAA	1.0	51 (15–119)
	CNA4B	4: 1021855–1022020	ATCC	HEX- CGGATGAGATGGAAAGAAGG	GTGCGTCTGTCAAAAGATTGC	0.3	10 (5–25)
	CNA4C	14: 131866–132031	TATT	TET- AGATGTCCTGGCGATGTTG	GAGGAGCAAGCAATCAAACC	0.3	11 (1–18)

^*The underlined residue(s) are not a match to the genomic sequence. These were introduced to minimize the formation of minus A peaks, a well known PCR artifact that may complicate interpretation of the results [34].